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The Work of the General Pharmaceutical Council
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Recommandé
Presented by Veronica Scola from the TGA, at the Coordinating Office for Clinical Trial Research Annual Workshop, 3 May 2017.
TGA Presentation: Using the online Clinical Trial Notification (CTN) form
TGA Presentation: Using the online Clinical Trial Notification (CTN) form
TGA Australia
To provide sponsors of OTC codeine products with information on how to submit an application to change the class of their product from OTC to prescription medicine
TGA presentation: Codeine Industry Forum - Regulatory options for up-scheduling
TGA presentation: Codeine Industry Forum - Regulatory options for up-scheduling
TGA Australia
Regulatory affairs
Regulatory affairs
Marina Hurtado Mira
To provide prescription medicines regulatory affairs personnel with information on development of the new minor variations e-form.
TGA Presentation: New e-form for minor variations
TGA Presentation: New e-form for minor variations
TGA Australia
The Regulatory system for complementary medicines.
Regulatory Authorities for Pharmaceuticals - TGA,MHRA,MCC
Regulatory Authorities for Pharmaceuticals - TGA,MHRA,MCC
Sanket Shinde
This presentation outlines reforms to the device regulatory system following the Expert Panel Review of Medicines and Medical Devices Regulation, reforms to the in vitro diagnostic devices (IVD) regulatory framework, reforms to the European and IVD system and the TGA's new Clinical Evidence Guidelines.
TGA presentation: AusMedtech, 24 May 2017
TGA presentation: AusMedtech, 24 May 2017
TGA Australia
Using the TGA Business Services Portal to apply for manufacturing licences and variations for biologicals.
TGA Licensing & Certification Applications: TGA Business Services Portal for ...
TGA Licensing & Certification Applications: TGA Business Services Portal for ...
TGA Australia
Outsourcing is a Cost-effective strategy when used properly and at present is gaining more and more importance. Here's a short presentation about the importance of outsourcing in Clinical research.
Outsourcing in Clinical Research
Outsourcing in Clinical Research
Mansi Gaikwad
Recommandé
Presented by Veronica Scola from the TGA, at the Coordinating Office for Clinical Trial Research Annual Workshop, 3 May 2017.
TGA Presentation: Using the online Clinical Trial Notification (CTN) form
TGA Presentation: Using the online Clinical Trial Notification (CTN) form
TGA Australia
To provide sponsors of OTC codeine products with information on how to submit an application to change the class of their product from OTC to prescription medicine
TGA presentation: Codeine Industry Forum - Regulatory options for up-scheduling
TGA presentation: Codeine Industry Forum - Regulatory options for up-scheduling
TGA Australia
Regulatory affairs
Regulatory affairs
Marina Hurtado Mira
To provide prescription medicines regulatory affairs personnel with information on development of the new minor variations e-form.
TGA Presentation: New e-form for minor variations
TGA Presentation: New e-form for minor variations
TGA Australia
The Regulatory system for complementary medicines.
Regulatory Authorities for Pharmaceuticals - TGA,MHRA,MCC
Regulatory Authorities for Pharmaceuticals - TGA,MHRA,MCC
Sanket Shinde
This presentation outlines reforms to the device regulatory system following the Expert Panel Review of Medicines and Medical Devices Regulation, reforms to the in vitro diagnostic devices (IVD) regulatory framework, reforms to the European and IVD system and the TGA's new Clinical Evidence Guidelines.
TGA presentation: AusMedtech, 24 May 2017
TGA presentation: AusMedtech, 24 May 2017
TGA Australia
Using the TGA Business Services Portal to apply for manufacturing licences and variations for biologicals.
TGA Licensing & Certification Applications: TGA Business Services Portal for ...
TGA Licensing & Certification Applications: TGA Business Services Portal for ...
TGA Australia
Outsourcing is a Cost-effective strategy when used properly and at present is gaining more and more importance. Here's a short presentation about the importance of outsourcing in Clinical research.
Outsourcing in Clinical Research
Outsourcing in Clinical Research
Mansi Gaikwad
Prescription medicines Minor Variation electronic form
Presentation: New e-form for minor variations: Prescription medicines
Presentation: New e-form for minor variations: Prescription medicines
TGA Australia
Pharmaceutical Regulatory Affairs Project 2015. Research Supervisor: Professor Peivand Pirouzi, Ph.D., M.B.A., Canada
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Pharmaceutical Compliance Inspection unit, Crown College of Canada
Inpatient Pharmacy Self Assessment
Inpatient Pharmacy Self Assessment
Diana Rangaves, PharmD, CEO
The presentation outlines how the TGA’s new priority review pathway for prescription medicines works and how medicines might be deemed to be a priority for Australian patients. We discuss how the provisional approval pathway contributes to early access and how to judge when early data seems promising.
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
TGA Australia
An overview of why and how the TGA collaborates with international organisations, including examples.
TGA Presentation: International collaboration – Why and with whom?
TGA Presentation: International collaboration – Why and with whom?
TGA Australia
Learn about our comprehensive pharmacy solutions at the point of care that allow physicians to improve clinical outcomes and increase patient satisfaction.
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
danielbrain10
Learn about our comprehensive pharmacy solutions at the point of care that allow physicians to improve clinical outcomes and increase patient satisfaction.
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
danielbrain10
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell,
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
The Partnership For Safe Medicines
3 hr virtual seminar china compliance processes for life science products
3 hr virtual seminar china compliance processes for life science products
complianceonline123
Drug Regulatory Affairs Introduction
Drug Regulatory Affairs
Drug Regulatory Affairs
Namdeo Shinde
drug regulatory affaris
Drug regulatory affairs - 1
Drug regulatory affairs - 1
Tanuja Bisht
This presentation provides an overview of the TGA’s post-market compliance program and how data from the program is used to manage non-compliance and highlight areas of concern.
How do listed medicines shape up in the post market compliance space
How do listed medicines shape up in the post market compliance space
TGA Australia
This slide cover basic aspects , regulatory body and marketing authorisation process in uk and European union.
Medicines and Healthcare products Regulatory Agency(MHRA)
Medicines and Healthcare products Regulatory Agency(MHRA)
Rishabh Agrawal
This presentation will inform you of all you need to know about the Pharmacy Technician program offer by Phoenix College Downtown
Pharmacy Technician Orientation
Pharmacy Technician Orientation
guestb9336a
Pharmacy Practice Regulations, 2015
Pharmacy practice regulations, 2015
Pharmacy practice regulations, 2015
Pharmacy
An overview of reform initiatives relevant to complementary medicines arising from the Review of Medicines and Medical Devices Regulation.
Presentation: Spotlight on complementary medicines MMDR reforms
Presentation: Spotlight on complementary medicines MMDR reforms
TGA Australia
Regulatory affair - Introduction, useful presentation for UG and PG students
Regulatory affair - Introduction
Regulatory affair - Introduction
Dr. Jigar Vyas
An overview of recent and current reforms to prescription medicines regulation in Australia
Presentation: Prescription Medicines Reforms
Presentation: Prescription Medicines Reforms
TGA Australia
Vigi flow -_data_entry
Vigi flow -_data_entry
Somnath Mondal
A discussion on the inspections close-out process, performance metrics and outcomes, inspection compliance outcomes, risk management, monitoring compliance, and common deficiencies found on inspections.
TGA Presentation: Data Metrics and Current Inspection Trends
TGA Presentation: Data Metrics and Current Inspection Trends
TGA Australia
What are Supergenerics, presentation by Dr Anthony Melvin Crasto
What are Supergenerics
What are Supergenerics
Anthony Melvin Crasto Ph.D
Charlotte City Council Meeting Minutes, January 26, 2009
Charlotte City Council Meeting Minutes, January 26, 2009
Daniel X. O'Neil
Contenu connexe
Tendances
Prescription medicines Minor Variation electronic form
Presentation: New e-form for minor variations: Prescription medicines
Presentation: New e-form for minor variations: Prescription medicines
TGA Australia
Pharmaceutical Regulatory Affairs Project 2015. Research Supervisor: Professor Peivand Pirouzi, Ph.D., M.B.A., Canada
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Pharmaceutical Compliance Inspection unit, Crown College of Canada
Inpatient Pharmacy Self Assessment
Inpatient Pharmacy Self Assessment
Diana Rangaves, PharmD, CEO
The presentation outlines how the TGA’s new priority review pathway for prescription medicines works and how medicines might be deemed to be a priority for Australian patients. We discuss how the provisional approval pathway contributes to early access and how to judge when early data seems promising.
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
TGA Australia
An overview of why and how the TGA collaborates with international organisations, including examples.
TGA Presentation: International collaboration – Why and with whom?
TGA Presentation: International collaboration – Why and with whom?
TGA Australia
Learn about our comprehensive pharmacy solutions at the point of care that allow physicians to improve clinical outcomes and increase patient satisfaction.
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
danielbrain10
Learn about our comprehensive pharmacy solutions at the point of care that allow physicians to improve clinical outcomes and increase patient satisfaction.
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
danielbrain10
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell,
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
The Partnership For Safe Medicines
3 hr virtual seminar china compliance processes for life science products
3 hr virtual seminar china compliance processes for life science products
complianceonline123
Drug Regulatory Affairs Introduction
Drug Regulatory Affairs
Drug Regulatory Affairs
Namdeo Shinde
drug regulatory affaris
Drug regulatory affairs - 1
Drug regulatory affairs - 1
Tanuja Bisht
This presentation provides an overview of the TGA’s post-market compliance program and how data from the program is used to manage non-compliance and highlight areas of concern.
How do listed medicines shape up in the post market compliance space
How do listed medicines shape up in the post market compliance space
TGA Australia
This slide cover basic aspects , regulatory body and marketing authorisation process in uk and European union.
Medicines and Healthcare products Regulatory Agency(MHRA)
Medicines and Healthcare products Regulatory Agency(MHRA)
Rishabh Agrawal
This presentation will inform you of all you need to know about the Pharmacy Technician program offer by Phoenix College Downtown
Pharmacy Technician Orientation
Pharmacy Technician Orientation
guestb9336a
Pharmacy Practice Regulations, 2015
Pharmacy practice regulations, 2015
Pharmacy practice regulations, 2015
Pharmacy
An overview of reform initiatives relevant to complementary medicines arising from the Review of Medicines and Medical Devices Regulation.
Presentation: Spotlight on complementary medicines MMDR reforms
Presentation: Spotlight on complementary medicines MMDR reforms
TGA Australia
Regulatory affair - Introduction, useful presentation for UG and PG students
Regulatory affair - Introduction
Regulatory affair - Introduction
Dr. Jigar Vyas
An overview of recent and current reforms to prescription medicines regulation in Australia
Presentation: Prescription Medicines Reforms
Presentation: Prescription Medicines Reforms
TGA Australia
Vigi flow -_data_entry
Vigi flow -_data_entry
Somnath Mondal
A discussion on the inspections close-out process, performance metrics and outcomes, inspection compliance outcomes, risk management, monitoring compliance, and common deficiencies found on inspections.
TGA Presentation: Data Metrics and Current Inspection Trends
TGA Presentation: Data Metrics and Current Inspection Trends
TGA Australia
Tendances
(20)
Presentation: New e-form for minor variations: Prescription medicines
Presentation: New e-form for minor variations: Prescription medicines
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Pharmaceutical Global Regulatory Affairs: Spain - by Aalmudena Camacho 2015
Inpatient Pharmacy Self Assessment
Inpatient Pharmacy Self Assessment
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
Presentation: Updates from the Therapeutic Goods Administration - For medicin...
TGA Presentation: International collaboration – Why and with whom?
TGA Presentation: International collaboration – Why and with whom?
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
Comprehensive pharmacy services | Point of care
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
The UK (MHRA) approach to combating Falsified Medicines by Gerald Heddell, MHRA
3 hr virtual seminar china compliance processes for life science products
3 hr virtual seminar china compliance processes for life science products
Drug Regulatory Affairs
Drug Regulatory Affairs
Drug regulatory affairs - 1
Drug regulatory affairs - 1
How do listed medicines shape up in the post market compliance space
How do listed medicines shape up in the post market compliance space
Medicines and Healthcare products Regulatory Agency(MHRA)
Medicines and Healthcare products Regulatory Agency(MHRA)
Pharmacy Technician Orientation
Pharmacy Technician Orientation
Pharmacy practice regulations, 2015
Pharmacy practice regulations, 2015
Presentation: Spotlight on complementary medicines MMDR reforms
Presentation: Spotlight on complementary medicines MMDR reforms
Regulatory affair - Introduction
Regulatory affair - Introduction
Presentation: Prescription Medicines Reforms
Presentation: Prescription Medicines Reforms
Vigi flow -_data_entry
Vigi flow -_data_entry
TGA Presentation: Data Metrics and Current Inspection Trends
TGA Presentation: Data Metrics and Current Inspection Trends
En vedette
What are Supergenerics, presentation by Dr Anthony Melvin Crasto
What are Supergenerics
What are Supergenerics
Anthony Melvin Crasto Ph.D
Charlotte City Council Meeting Minutes, January 26, 2009
Charlotte City Council Meeting Minutes, January 26, 2009
Daniel X. O'Neil
CPS Council Presentation
CPS Council Presentation May 2016
CPS Council Presentation May 2016
Community Pharmacy Scotland
In this presentation from, Janeen Santorosa discusses the best practices for harmonization of GMP auditing, domestic and international regulations for supplier auditing, integration of risk-based practices, and supplier audit practice tools.
Incorporate Domestic and International Regulations for Effective GMP Auditing
Incorporate Domestic and International Regulations for Effective GMP Auditing
Institute of Validation Technology
This full day presentation gives an overview of the process validation lifecycle approach, the FDA PV Guidance, the lifecycle approach to cleaning validation, equipment qualification, and validation quality systems.
Validation Boot Camp
Validation Boot Camp
Institute of Validation Technology
Follow the CPS Council Meeting for Nov 2016 online.
CPS Council Meeting - November 2016
CPS Council Meeting - November 2016
Kirsten Crawford
A reflection on progress made, and challenges to be addressed, in realizing the desired state articulated by the the FDA Initiative on Pharmaceutical Quality for the 21st Century.
Pharmaceutical Product & Process Design & Quality
Pharmaceutical Product & Process Design & Quality
Ajaz Hussain
This Annex describes the principles of qualification and validation which are applicable to the facilities, equipment, utilities and processes used for the manufacture of medicinal products and may also be used as supplementary optional guidance for active substances without introduction of additional requirements to EudraLex, Volume 4, Part II. It is a GMP requirement that manufacturers control the critical aspects of their particular operations through qualification and validation over the life cycle of the product and process. Any planned changes to the facilities, equipment, utilities and processes, which may affect the quality of the product, should be formally documented and the impact on the validated status or control strategy assessed. Computerised systems used for the manufacture of medicinal products should also be validated according to the requirements of Annex 11. The relevant concepts and guidance presented in ICH Q8, Q9, Q10 and Q11 should also be taken into account. Highlights of the guidance are given in following presentation.
New EU Requirements for Qualification & Validation
New EU Requirements for Qualification & Validation
GMP EDUCATION : Not for Profit Organization
FDA Process Validation Guidance (Guidance for Industry: Process Validation- General Principles and Practices, Jan. 2011) outlines process validation activities in three stages - Stage 1: Process Design, Stage 2: Process Qualification and Stage 3: Continued Process Verification. Completion of Stage 2 subsequent to Stage 1 is a major milestone in the Process Validation Lifecycle as it confirms the process design and demonstrates the expected consistent performance of the manufacturing process. Knowledge and information gained from the design stage through the process qualification stage is used to complete this assessment. Stage 2 demonstrates suitability for successful commercial distribution where the data indicates that the process meets the conditions established in the protocol. Continued Process Verification is initiated for the subsequent commercial batches. Stage 3 assures that the process remains in a state of control during commercial manufacture. This presentation gives a practical approach to implement the stage 3 of the FDA Process Validation Guide.
US FDA Process Validation Stage 3: Continued Process Verification
US FDA Process Validation Stage 3: Continued Process Verification
GMP EDUCATION : Not for Profit Organization
Pharmaceutical quality decisions are made by multidisciplinary teams (a range of maturity), at different times and in various organizations; understanding of the QbD paradigm and methodology is derived experientially -One Quality Voice is hard to achieve! Legacy challenges, various ontological assumptions, and weak epistemology curtails knowledge sharing, delays consensus and keeps us trapped in a reactive mode (3rd Order) The risk of irrational decision making needs to be accounted. ”Cut-paste” or “check-the-box” practices are reminders that we are not achieving an optimal integration or practicing systems thinking. A reactive approach (3rd Order) to filling the noted gaps poses risk of continued erosion in the confidence the public should have in our assurance of pharmaceutical quality We need a thoughtful, planned approach to filling these gaps –NIPTE should take on this challenge! Will it?
NIPTE Conference 2016 Keynote Ajaz Hussain 09272016 Final
NIPTE Conference 2016 Keynote Ajaz Hussain 09272016 Final
Ajaz Hussain
This presentation give a detailed overview of the PICS draft guidance on Data Integrity and Management.
New PICS Guidance on Data Integrity and Management.
New PICS Guidance on Data Integrity and Management.
GMP EDUCATION : Not for Profit Organization
Educational presentation for administrative professionals just learning, or wanting to improve their minute-taking skills.
Minute by Minute: Learning the Skill of Taking Meeting Minutes
Minute by Minute: Learning the Skill of Taking Meeting Minutes
Beckie Layton
Drug discovery, hit to lead by DR ANTHONY MELVIN CRASTO
Drug discovery hit to lead
Drug discovery hit to lead
Anthony Melvin Crasto Ph.D
8 Modules of leadership Development
Leadership Deveopment Brochure
Leadership Deveopment Brochure
Laurence Yap M.A. (UM) CHRM
This presentation highlights how Risk Assessment can be used to control Elemental Impurities. in Drug Products.
Risk Assessment for Control of Elemental Impurities.
Risk Assessment for Control of Elemental Impurities.
GMP EDUCATION : Not for Profit Organization
Chapter 15 community pharmacy
Chapter 15 community pharmacy
Ann Bentley
venkybunnyt@gmail.com
problems in tablet manufacturing and coating
problems in tablet manufacturing and coating
venkatesh thota
Facilitation skills
Basic Facilitation Skills
Basic Facilitation Skills
Laurence Yap M.A. (UM) CHRM
QbD by Dr Anthony crasto, a brief review for API
Qbd by Anthony Melvin Crasto for API
Qbd by Anthony Melvin Crasto for API
Anthony Melvin Crasto Ph.D
Accelerating Generic Approvals, keys to be the first in market, With reference to CRO'S
Accelerating Generic Approvals by Dr Anthony Crasto
Accelerating Generic Approvals by Dr Anthony Crasto
Anthony Melvin Crasto Ph.D
En vedette
(20)
What are Supergenerics
What are Supergenerics
Charlotte City Council Meeting Minutes, January 26, 2009
Charlotte City Council Meeting Minutes, January 26, 2009
CPS Council Presentation May 2016
CPS Council Presentation May 2016
Incorporate Domestic and International Regulations for Effective GMP Auditing
Incorporate Domestic and International Regulations for Effective GMP Auditing
Validation Boot Camp
Validation Boot Camp
CPS Council Meeting - November 2016
CPS Council Meeting - November 2016
Pharmaceutical Product & Process Design & Quality
Pharmaceutical Product & Process Design & Quality
New EU Requirements for Qualification & Validation
New EU Requirements for Qualification & Validation
US FDA Process Validation Stage 3: Continued Process Verification
US FDA Process Validation Stage 3: Continued Process Verification
NIPTE Conference 2016 Keynote Ajaz Hussain 09272016 Final
NIPTE Conference 2016 Keynote Ajaz Hussain 09272016 Final
New PICS Guidance on Data Integrity and Management.
New PICS Guidance on Data Integrity and Management.
Minute by Minute: Learning the Skill of Taking Meeting Minutes
Minute by Minute: Learning the Skill of Taking Meeting Minutes
Drug discovery hit to lead
Drug discovery hit to lead
Leadership Deveopment Brochure
Leadership Deveopment Brochure
Risk Assessment for Control of Elemental Impurities.
Risk Assessment for Control of Elemental Impurities.
Chapter 15 community pharmacy
Chapter 15 community pharmacy
problems in tablet manufacturing and coating
problems in tablet manufacturing and coating
Basic Facilitation Skills
Basic Facilitation Skills
Qbd by Anthony Melvin Crasto for API
Qbd by Anthony Melvin Crasto for API
Accelerating Generic Approvals by Dr Anthony Crasto
Accelerating Generic Approvals by Dr Anthony Crasto
Similaire à The Work of the General Pharmaceutical Council
The clinical establishments act was adopted in year 2012, still so many states are to implement this act. This act is equally applicable for all system of medicine including Ayurveda. Here are the standards for ayurveda clinics and hospital. Present presentation explain the standards for ayurvedic clinics and dispensaries only
Clinical establishments act and Standard for Ayurvedic Clinics
Clinical establishments act and Standard for Ayurvedic Clinics
Dr.Surendra Chaudhary
CoArtha Technolsolutions IT for Meaningful Use
CoArtha Technolsolutions IT for Meaningful Use
MapRecruit.com
CLINICAL DATA MANAGEMENT SYSTEM
Clinical research management slide
Clinical research management slide
akashgayakwad1
What are regulatory bodies:- In the present scenario, pharmaceuticals are considered as the most highly regulated industries worldwide. The regulatory body ensures compliances in various legal and regulatory aspects of a drug. Every country has its own regulatory authority, which is responsible to enforce the rules and regulations and issue the guidelines to regulate drug development process, licensing, registration, manufacturing. marketing and labeling of pharmaceutical products like: USFDA(USA) MHRA(UK) TGA(Australia AIMS:- Protecting public health through regulation, with acceptablebenefit-risk profiles for medicines and devices. Promoting public health by helping people who use these productsto understand their benefits and risks. Improving public health by encouraging and facilitating developments in products that will benefit people GUIDELINES:- Guidelines for Manufacturers on Clinical Investigations to be carried out in the UK. Inspected UK Contract GMP Quality Control Laboratories. BLUE GUIDE: Advertising and Promotion of medicines in the UK. ORANGE GUIDE: Rules and Guidelines for Pharmaceutical Manufacturers and Distributors. Good Pharmacovigilance Practice Guide. Guidelines on Process Validation Guide to UK GLP Regulations 1999 Recommendations on the control and monitoring of storage and transportation temperatures of medicinal products. Guide to defective medicinal products. Introduction of a Risk Based Inspection Programme for GMP Labs. SALIENT FEATURES, COMMITTEES/WORKING GROUPS:- MHRA has the power to withdraw a product from market and suspend production of medicines. A manufacturer or distributor can be prosecuted if the law has been broken. Regulatory decisions are impartial D Different products are treated differently. MHRA collaborates with : US Food and Drug Administration NPSA National Patient Safety Agency NICE National Institute for Health and Clinical Excellence
Medicines and Healthcare products Regulatory Agency(MHRA)
Medicines and Healthcare products Regulatory Agency(MHRA)
TMU
Pharmaceutical practice
Pharmaceutical practice
Abel Castillo II
Regulatory affairs
Regulatory affairs
sekhara
Retail Pharmacy Practice in Bangladesh and Abroad
Retail pharmacy practice in bangladesh and abroad
Retail pharmacy practice in bangladesh and abroad
MD Jahidul Islam
GRP
Good Regulatory Practices.pptx
Good Regulatory Practices.pptx
Sudipta Roy
Describes the meaning of the manual in simple words, need and scope of the manual in the hospitals and contents of it.
Hospital pharmacy procedural manual
Hospital pharmacy procedural manual
Devyani Joshi
Quality regulation for biological products current and future
Quality regulation for biological products current and future
National Institute of Biologics
this ppt is about all the rules and regulations of drugs in Japan.this ppt contains the PMDA structure, DMF data, IND and NDA procedure, cosmetic regulations, post marketing survelliance etc.
Regulatory requirnment and approval procedure of drugs in japan ppt
Regulatory requirnment and approval procedure of drugs in japan ppt
sandeep bansal
Hospital committees
Hospital committees
Hospital committees
DrSiddharthSingh5
Technology development and transfer: Approved regulatory bodies and agencies
4.2 TT-Approved regulatory bodies and agencies.pdf
4.2 TT-Approved regulatory bodies and agencies.pdf
ASSAM DOWN TOWN UNIVERSITY
Conference on Health and Social Protection: Meeting the needs of the poor, 9-10 October 2008 www.povill.com
Rolf Panel Syhakhang
Rolf Panel Syhakhang
IDS
Professor Peivand Pirouzi Inc. - Copyright 2015 - Professor Peivand Pirouzi Inc., International Corporate Training, Canada All rights reserved
Pharmaceutical Global Regulatory Affairs: Japan - by Jieun Lim and Mozhdeh Alemi
Pharmaceutical Global Regulatory Affairs: Japan - by Jieun Lim and Mozhdeh Alemi
Pharmaceutical Compliance Inspection unit, Crown College of Canada
Responsibilities and Functions of CDSCO
CDSCO.pptx
CDSCO.pptx
mamtakumari930473
A Report on Department of Drug Administration and National Medicine Laboratory visit
A Report on Department of Drug Administration and National Medicine Laborator...
A Report on Department of Drug Administration and National Medicine Laborator...
Nabin Bist
This presentation provided an overview of the regulation of complementary medicines.
The regulation of complementary medicines
The regulation of complementary medicines
TGA Australia
Quality assurance process
Quality assurance process final
Quality assurance process final
Rahibikram Thapa
Regulatory Control , Regulatory bodies
Quality assurance process final
Quality assurance process final
Kshitiz Thapa
Similaire à The Work of the General Pharmaceutical Council
(20)
Clinical establishments act and Standard for Ayurvedic Clinics
Clinical establishments act and Standard for Ayurvedic Clinics
CoArtha Technolsolutions IT for Meaningful Use
CoArtha Technolsolutions IT for Meaningful Use
Clinical research management slide
Clinical research management slide
Medicines and Healthcare products Regulatory Agency(MHRA)
Medicines and Healthcare products Regulatory Agency(MHRA)
Pharmaceutical practice
Pharmaceutical practice
Regulatory affairs
Regulatory affairs
Retail pharmacy practice in bangladesh and abroad
Retail pharmacy practice in bangladesh and abroad
Good Regulatory Practices.pptx
Good Regulatory Practices.pptx
Hospital pharmacy procedural manual
Hospital pharmacy procedural manual
Quality regulation for biological products current and future
Quality regulation for biological products current and future
Regulatory requirnment and approval procedure of drugs in japan ppt
Regulatory requirnment and approval procedure of drugs in japan ppt
Hospital committees
Hospital committees
4.2 TT-Approved regulatory bodies and agencies.pdf
4.2 TT-Approved regulatory bodies and agencies.pdf
Rolf Panel Syhakhang
Rolf Panel Syhakhang
Pharmaceutical Global Regulatory Affairs: Japan - by Jieun Lim and Mozhdeh Alemi
Pharmaceutical Global Regulatory Affairs: Japan - by Jieun Lim and Mozhdeh Alemi
CDSCO.pptx
CDSCO.pptx
A Report on Department of Drug Administration and National Medicine Laborator...
A Report on Department of Drug Administration and National Medicine Laborator...
The regulation of complementary medicines
The regulation of complementary medicines
Quality assurance process final
Quality assurance process final
Quality assurance process final
Quality assurance process final
Plus de IMI PQ NET Romania
Prezentare 27febr2014 dir201355
Prezentare 27febr2014 dir201355
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Pcu prezentare intercontinental
Pcu prezentare intercontinental
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Prezentare ghiduri si studii comparative anc conferinta final imipqnet finala
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Diseminare vizita de studiu in Portugalia
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European Professional Card
Epc in imi focus group pm
Epc in imi focus group pm
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Rezultate proiect imi pq net ro
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IMI PQ NET Romania
Ghidul de certificare şi recunoaştere pentru profesia de arhivist Autor: dr. ing. Ionel POPA 2013
Arhivist - Ionel Popa - Interne-justitie
Arhivist - Ionel Popa - Interne-justitie
IMI PQ NET Romania
GHID PRIVIND CERTIFICAREA COMPETENŢELOR ŞI RECUNOAŞTEREA CALIFICĂRILOR PENTRU AGENŢI DE ASIGURARE ŞI BROKERI ÎN ASIGURĂRI Autor: Dr. Irina Dumitriu Iulie 2013
Agent asigurare, Broker asigurari - Irina Dumitriu - Economic-financiar
Agent asigurare, Broker asigurari - Irina Dumitriu - Economic-financiar
IMI PQ NET Romania
Termeni referinta standard orientativi - Nicolae Ionescu, Irina Dumitriu
Termeni referinta standard orientativi - Nicolae Ionescu, Irina Dumitriu
IMI PQ NET Romania
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Tehnician veterinar - Alexandrina Sirbu - Agricultura-veterinar
Tehnician veterinar - Alexandrina Sirbu - Agricultura-veterinar
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENŢELOR ŞI DE RECUNOAŞTERE A CALIFICĂRILOR ÎN ITALIA Autor: Conf. Dr. Ing. Nicolae IONESCU 2013
Studiu comparativ Republica Italiana - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Nicolae Ionescu - iunie 2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENŢELOR ŞI DE RECUNOAŞTERE A CALIFICĂRILOR ÎN ITALIA ANEXA 2. PROFESII REGLEMENTATE ÎN ITALIA, AUTORITĂŢI COMPETENTE, PERSOANE DE CONTACT SI STATISTICI Autor: Conf. Dr. Ing. Nicolae IONESCU 2013
Studiu comparativ Republica Italiana - Anexa 2 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 2 - Nicolae Ionescu - iunie 2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENŢELOR ŞI DE RECUNOAŞTERE A CALIFICĂRILOR ÎN ITALIA ANEXA1. LISTA PROFESIILOR REGLEMENTATE ÎN ITALIA Autor: Conf. Dr. Ing. Nicolae IONESCU 2013
Studiu comparativ Republica Italiana - Anexa 1 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 1 - Nicolae Ionescu - iunie 2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENȚELOR ȘI DE RECUNOAȘTERE A CALIFICĂRILOR ÎN GERMANIA Autor: Prof.univ.dr.ing. Alexandrina Sîrbu 2013
Studiu comparativ Republica Federala Germania - Alexandrina Sirbu - iunie 2013
Studiu comparativ Republica Federala Germania - Alexandrina Sirbu - iunie 2013
IMI PQ NET Romania
Procesele de certificare a competenţelor şi de recunoaştere a calificărilor în Republica CEHĂ Autor: dr. ing. Ionel POPA 2013
Studiu comparativ Republica Ceha - Ionel Popa - iunie 2013
Studiu comparativ Republica Ceha - Ionel Popa - iunie 2013
IMI PQ NET Romania
Procesele de certificare a competenţelor şi de recunoaştere a calificărilor în Olanda Autor: Dr. Irina Dumitriu Martie 2013
Studiu comparativ Regatul Tarilor de jos - Olanda - Irina Dumitriu - iunie2013
Studiu comparativ Regatul Tarilor de jos - Olanda - Irina Dumitriu - iunie2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENȚELOR ȘI DE RECUNOAȘTERE A CALIFICĂRILOR ÎN SPANIA Autor: Prof.univ.dr.ing. Liviu Sevastian BOCÎI 2013
Studiu comparativ Regatul Spaniei - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Liviu Sevastian Bocii - iunie 2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENTELOR SI DE RECUNOASTERE A CALIFICARILOR IN SPANIA Anexa 2 . Profesiile reglementate din România și Autoritățile Competente corespondente Autor: Prof.univ.dr.ing. Liviu Sevastian BOCÎI 2013
Studiu comparativ Regatul Spaniei - Anexa 2 - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 2 - Liviu Sevastian Bocii - iunie 2013
IMI PQ NET Romania
PROCESELE DE CERTIFICARE A COMPETENTELOR SI DE RECUNOASTERE A CALIFICARILOR IN SPANIA Anexa 1. Profesiile reglementate din Spania Autor: Prof.univ.dr.ing. Liviu Sevastian BOCÎI 2013
Studiu comparativ Regatul Spaniei - Anexa 1 - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 1 - Liviu Sevastian Bocii - iunie 2013
IMI PQ NET Romania
Plus de IMI PQ NET Romania
(20)
Prezentare 27febr2014 dir201355
Prezentare 27febr2014 dir201355
Pcu prezentare intercontinental
Pcu prezentare intercontinental
Prezentare ghiduri si studii comparative anc conferinta final imipqnet finala
Prezentare ghiduri si studii comparative anc conferinta final imipqnet finala
Diseminare vizita de studiu in Portugalia
Diseminare vizita de studiu in Portugalia
Epc in imi focus group pm
Epc in imi focus group pm
Rezultate proiect imi pq net ro
Rezultate proiect imi pq net ro
Medic - Camelia Szuhanek - Sanatate
Medic - Camelia Szuhanek - Sanatate
Arhivist - Ionel Popa - Interne-justitie
Arhivist - Ionel Popa - Interne-justitie
Agent asigurare, Broker asigurari - Irina Dumitriu - Economic-financiar
Agent asigurare, Broker asigurari - Irina Dumitriu - Economic-financiar
Termeni referinta standard orientativi - Nicolae Ionescu, Irina Dumitriu
Termeni referinta standard orientativi - Nicolae Ionescu, Irina Dumitriu
Tehnician veterinar - Alexandrina Sirbu - Agricultura-veterinar
Tehnician veterinar - Alexandrina Sirbu - Agricultura-veterinar
Studiu comparativ Republica Italiana - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 2 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 2 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 1 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Italiana - Anexa 1 - Nicolae Ionescu - iunie 2013
Studiu comparativ Republica Federala Germania - Alexandrina Sirbu - iunie 2013
Studiu comparativ Republica Federala Germania - Alexandrina Sirbu - iunie 2013
Studiu comparativ Republica Ceha - Ionel Popa - iunie 2013
Studiu comparativ Republica Ceha - Ionel Popa - iunie 2013
Studiu comparativ Regatul Tarilor de jos - Olanda - Irina Dumitriu - iunie2013
Studiu comparativ Regatul Tarilor de jos - Olanda - Irina Dumitriu - iunie2013
Studiu comparativ Regatul Spaniei - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 2 - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 2 - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 1 - Liviu Sevastian Bocii - iunie 2013
Studiu comparativ Regatul Spaniei - Anexa 1 - Liviu Sevastian Bocii - iunie 2013
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In this webinar, members learned the ABCs of keeping books for a nonprofit organization. Some of the key takeaways were: - What is accounting and how does it work? - How do you read a financial statement? - What are the three things that nonprofits are required to track? -And more
Introduction to Nonprofit Accounting: The Basics
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TechSoup
In this webinar, nonprofits learned how to delve into the minds of funders, unveiling what they truly seek in qualified grant applicants, and tools for success. Learn more about the Grant Readiness Review service by Remy Consulting at TechSoup to help you gather, organize, and assess the strength of documents required for grant applications.
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Andreas Schleicher, Director for Education and Skills at the OECD, presents at the webinar No Child Left Behind: Tackling the School Absenteeism Crisis on 30 April 2024.
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
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EduSkills OECD
Russian Escort Service in Delhi 11k Hotel Foreigner Russian Call Girls in Delhi Welcome to VIP Call Girl In Delhi Hello! Delhi Call Girls is one of the most popular cities in India. Girls who call in Delhi frequently Advertise their services in small promgons in magazines, as well as on the Internet but We do not act as a direct-promoter. We will do everything we can to make sure that you're safe to the max to the best of our abilities and making sure of our ability and ensuring that you're obtained to the best of our abilities and making sure that you get what you want. Sexuality of our females is recognized by our Business proposals. Top-of-the-line, fully-featured Delhi girl call number and we offer To be aware of it is a major reason in deciding to use our services to ensure that our customers realize the worth of their lives swiftly and in a pleasant manner by engaging with web series performers for a cost of 10000.Here you are able to be Relax knowing that personal information is stored in the business proposals, giving an appearance of like you're as if you are a full affirmation. Call Girls Service Now Delhi +91-9899900591 *********** N.M.************* 01/04/2024 ▬█⓿▀█▀ 𝐈𝐍𝐃𝐄𝐏𝐄𝐍𝐃𝐄𝐍𝐓 CALL 𝐆𝐈𝐑𝐋 𝐕𝐈𝐏 𝐄𝐒𝐂𝐎𝐑𝐓 SERVICE ✅ ❣️ ⭐➡️HOT & SEXY MODELS // COLLEGE GIRLS AVAILABLE FOR COMPLETE ENJOYMENT WITH HIGH PROFILE INDIAN MODEL AVAILABLE HOTEL & HOME ★ SAFE AND SECURE HIGH CLASS SERVICE AFFORDABLE RATE ★ SATISFACTION,UNLIMITED ENJOYMENT. ★ All Meetings are confidential and no information is provided to any one at any cost. ★ EXCLUSIVE PROFILes Are Safe and Consensual with Most Limits Respected ★ Service Available In: - HOME & HOTEL Star Hotel Service .In Call & Out call SeRvIcEs : ★ A-Level (star escort) ★ Strip-tease ★ BBBJ (Bareback Blowjob)Receive advanced sexual techniques in different mode make their life more pleasurable. ★ Spending time in hotel rooms ★ BJ (Blowjob Without a Condom) ★ Completion (Oral to completion) ★ Covered (Covered blowjob Without condom SAFE AND SECURE
Russian Escort Service in Delhi 11k Hotel Foreigner Russian Call Girls in Delhi
Russian Escort Service in Delhi 11k Hotel Foreigner Russian Call Girls in Delhi
kauryashika82
This presentation was provided by William Mattingly of the Smithsonian Institution, during the third segment of the NISO training series "AI & Prompt Design." Session Three: Beginning Conversations, was held on April 18, 2024.
Mattingly "AI & Prompt Design: The Basics of Prompt Design"
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National Information Standards Organization (NISO)
My CV as of the end of April 2024
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agholdier
Students will get the knowledge of the following- meaning of the pricing, its importance, objectives, methods of pricing, factors affecting the price of products, An overview of DPCO (Drug Price Control Order) and NPPA (National Pharmaceutical Pricing Authority)
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MBA Sem 4 | Business Analytics [BA 4] | Previous Year Question Paper | Summer 2023 | Web and Social Media Analytics | Solved PYQ | By Jayanti Pande | ProNotesJRP
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ciinovamais
In Bachelor of Pharmacy course, Class- 1st year, sem-II Subject EVS having topic of ECOLOGICAL SUCCESSION under the ECOSYSTEM point in this presentation points like ecological succession , types of ecological succession like primary and secondary explain with diagram. Students having deep knowledge about Ecological Succession after studying this presentation.
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Basic Civil Engineering notes first year Notes Building notes Selection of site for Building Layout of a Building What is Burjis, Mutam Building Bye laws Basic Concept of sunlight ventilation in building National Building Code of India Set back or building line Types of Buildings Floor Space Index (F.S.I) Institutional Vs Educational Building Components & function Sills, Lintels, Cantilever Doors, Windows and Ventilators Types of Foundation AND THEIR USES Plinth Area Shallow and Deep Foundation Super Built-up & carpet area Floor Area Ratio (F.A.R) RCC Reinforced Cement Concrete RCC VS PCC
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This presentation was provided by William Mattingly of the Smithsonian Institution, during the fourth segment of the NISO training series "AI & Prompt Design." Session Four: Structured Data and Assistants, was held on April 25, 2024.
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Unit-IV- Pharma. Marketing Channels.pptx
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The global implications of DORA and NIS 2 Directive are significant, extending beyond the European Union. Amongst others, the webinar covers: • DORA and its Implications • Nis 2 Directive and its Implications • How to leverage directive and regulation as a marketing tool and competitive advantage • How to use new compliance framework to request additional budget Presenters: Christophe Mazzola - Senior Cyber Governance Consultant Armed with endless Excel files, a meme catalog worthy of the best X'os (formerly twittos), and a risk register to make your favorite risk manager jealous, I swapped my computer scientist cape a few years ago for that of a (cyber) threat hunter with the honorary title of CISO. Ah, and I am also a quadruple senior certified ISO27001/2/5, Pas mal non ? C'est francais. Malcolm Xavier Malcolm Xavier has been working in the Digital Industry for over 18 Years now. He has worked with Global Clients in South Africa, United States and United Kingdom. He has achieved Many Professional Certifications Like CISSP, Google Cloud Practitioner, TOGAF, Azure Cloud, ITIL v3 etc. His core competencies include IT strategy, cybersecurity, IT infrastructure management, data center migration and consolidation, data protection and compliance, risk management and governance, and IS program development and management. Date: April 25, 2024 Tags: Information Security, Digital Operational Resilience Act (DORA) ------------------------------------------------------------------------------- Find out more about ISO training and certification services Training: Digital Operational Resilience Act (DORA) - EN | PECB NIS 2 Directive - EN | PECB Webinars: https://pecb.com/webinars Article: https://pecb.com/article Whitepaper: https://pecb.com/whitepaper ------------------------------------------------------------------------------- For more information about PECB: Website: https://pecb.com/ LinkedIn: https://www.linkedin.com/company/pecb/ Facebook: https://www.facebook.com/PECBInternational/ Slideshare: http://www.slideshare.net/PECBCERTIFICATION
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Basic Civil Engineering first year Notes- Chapter 4 Building.pptx
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Mattingly "AI & Prompt Design: Structured Data, Assistants, & RAG"
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Unit-IV- Pharma. Marketing Channels.pptx
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The Work of the General Pharmaceutical Council
1.
The work of
the General Pharmaceutical Council [GPhC] October 2011
2.
3.
Set standards
4.
5.
Education & training
6.
Pharmacists
7.
Pharmacy Technicians
8.
Pharmacy support staff
9.
Levels
10.
11.
How standards fit
in
12.
13.
The Register
14.
15.
16.
17.
CPD
18.
19.
Fitness to practise
20.
The process
21.
22.
23.
The Inspectorate
24.
25.
26.
Standards advisory team
[pharmacists]
27.
28.
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