Soumettre la recherche
Mettre en ligne
Excipient Auditing
•
Télécharger en tant que PPT, PDF
•
1 j'aime
•
1,388 vues
John E. Osani
Suivre
Signaler
Partager
Signaler
Partager
1 sur 42
Télécharger maintenant
Recommandé
Good manufacturing practices (gmp) for pharmaceutical excipients
Good manufacturing practices (gmp) for pharmaceutical excipients
Durgasai Relangi
Audit
Audit
Prasenjit Mondal
Six system inspection is a part of pharmaceutical.management system.this presentation gives the information about production, facilities and equipment, quality, laboratory,packaging and material system.
Six system of inspection quality assurance
Six system of inspection quality assurance
Learning is a habit
change control application in pharma industry
Change control
Change control
ratan mukhopadhyay
fundamental principles and types of quality assurance audits
quality assurance audits
quality assurance audits
rasikawalunj
A Seminar On Quality Audit Prepared by :- Chaitrali D.Gole M.Ph (Q.A Sem-1) R.D.C.O.P Bhor.
Quality audit slideshare
Quality audit slideshare
chaitrali1995
cGMP Training: Deviation handling is important area to reporting and investigation & documentation.
GMP Training: Handling of deviation
GMP Training: Handling of deviation
Dr. Amsavel A
It is detailed presentation for auditors to perform GMP trainings & audits
Gmp Auditor Training Course
Gmp Auditor Training Course
piyush64173
Recommandé
Good manufacturing practices (gmp) for pharmaceutical excipients
Good manufacturing practices (gmp) for pharmaceutical excipients
Durgasai Relangi
Audit
Audit
Prasenjit Mondal
Six system inspection is a part of pharmaceutical.management system.this presentation gives the information about production, facilities and equipment, quality, laboratory,packaging and material system.
Six system of inspection quality assurance
Six system of inspection quality assurance
Learning is a habit
change control application in pharma industry
Change control
Change control
ratan mukhopadhyay
fundamental principles and types of quality assurance audits
quality assurance audits
quality assurance audits
rasikawalunj
A Seminar On Quality Audit Prepared by :- Chaitrali D.Gole M.Ph (Q.A Sem-1) R.D.C.O.P Bhor.
Quality audit slideshare
Quality audit slideshare
chaitrali1995
cGMP Training: Deviation handling is important area to reporting and investigation & documentation.
GMP Training: Handling of deviation
GMP Training: Handling of deviation
Dr. Amsavel A
It is detailed presentation for auditors to perform GMP trainings & audits
Gmp Auditor Training Course
Gmp Auditor Training Course
piyush64173
Second Party Audit:- Second-party audit is when a company performs an audit of a supplier to ensure that they are meeting the requirements specified in the contract. External Third Party Audit:- A third-party audit occurs when a company has decided that they want to create a Quality Management System (QMS) that conforms to a standard set of requirements, such as ISO 9001 and hire an independent auditing company to perform an audit to verify that the company has succeeded in meeting these standards.
Second Party Audit and External Third Party Audit
Second Party Audit and External Third Party Audit
ShantanuThakre3
IMPORTANCE OF QUALITY SYSTEM
Change control oos oot
Change control oos oot
AMOGH DANDEKAR
Quality & GMP Presentation
Quality & GMP Presentation
mayydabajwa
This contains all about Quality Management System
2) Total Quality Managment
2) Total Quality Managment
Sangam Kanthale
Quality Systems Approach to Pharmaceutical cGMP
Quality Systems Approach to Pharmaceutical cGMP
Reddy N
Sir. M. S. Gosavi College of pharmaceutical education Nashik
Quality control grp.7 (49-56)
Quality control grp.7 (49-56)
AkankshaLunge
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
ceutics1315
QA: It is the sum total of the organized arrangements with the objective of ensuring that products will be of the quality required for their intended. GMP: Part of QA which ensures that products are consistently produced & controlled to the quality standards appropriate to their use. GMP is an integral part of QA.
Qc, qa
Qc, qa
Poornima Santhosh
Quality control in pharmaceutical Industry
Quality Control in Pharmaceutical Industry
Quality Control in Pharmaceutical Industry
Prashant Tomar
G m p 01
G m p 01
saravanan vaidyanathan
for capsules and sterile products
Vendor Audit
Vendor Audit
PRAVADA
WHO Good Manufacturing Practice Requirements Good Manufacturing Practice is the part of quality assurance that ensures that products are consistently manufactured and controlled to the quality standards appropriate to their intended use.
WHO GMP Requirements
WHO GMP Requirements
Deekshitha HS
THIS PRESENTATION IS ABOUT THE CHANGE CONTROL IN PHARMACEUTICALS
CHANGE CONTROL
CHANGE CONTROL
sonia nazir
presentation on GMP training
Gmp change control by amsavel
Gmp change control by amsavel
Amsavel Vel
This presentation has been prepared from publicly available materials on the world wide web.
Product Quality Review (PQR)
Product Quality Review (PQR)
Rikul Patel
just for an idea
calulation of yields, production record review,change control
calulation of yields, production record review,change control
srikrupa institute of pharmaceutical analysis
TECHSHORE INSPECTION SERVICES|INSTITUTE OF QA/QC IN KERALA|ANTICIPATING CONSTRUCTION DEFECTS THROUGH EFFECTIVE QUALITY CONTROL
Qa qc course in Techshore inspection services
Qa qc course in Techshore inspection services
Techshore Inspection Services
Quality Assurance techniques
Emergent trends in QA of drug
Emergent trends in QA of drug
krushnakantwable
introduction About The Audits Of microbiological Laboretories
Auditing of microbiology laboratory
Auditing of microbiology laboratory
Nikita Amane
ICH Q10 guideline for pharmacutical industry.
ICH Q10
ICH Q10
Abu Naim Shekh
Responding To A 483and Warning Letter
Responding To A 483and Warning Letter
John E. Osani
PCrompton_Warning Letter Response
PCrompton_Warning Letter Response
Philip Crompton
Contenu connexe
Tendances
Second Party Audit:- Second-party audit is when a company performs an audit of a supplier to ensure that they are meeting the requirements specified in the contract. External Third Party Audit:- A third-party audit occurs when a company has decided that they want to create a Quality Management System (QMS) that conforms to a standard set of requirements, such as ISO 9001 and hire an independent auditing company to perform an audit to verify that the company has succeeded in meeting these standards.
Second Party Audit and External Third Party Audit
Second Party Audit and External Third Party Audit
ShantanuThakre3
IMPORTANCE OF QUALITY SYSTEM
Change control oos oot
Change control oos oot
AMOGH DANDEKAR
Quality & GMP Presentation
Quality & GMP Presentation
mayydabajwa
This contains all about Quality Management System
2) Total Quality Managment
2) Total Quality Managment
Sangam Kanthale
Quality Systems Approach to Pharmaceutical cGMP
Quality Systems Approach to Pharmaceutical cGMP
Reddy N
Sir. M. S. Gosavi College of pharmaceutical education Nashik
Quality control grp.7 (49-56)
Quality control grp.7 (49-56)
AkankshaLunge
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
ceutics1315
QA: It is the sum total of the organized arrangements with the objective of ensuring that products will be of the quality required for their intended. GMP: Part of QA which ensures that products are consistently produced & controlled to the quality standards appropriate to their use. GMP is an integral part of QA.
Qc, qa
Qc, qa
Poornima Santhosh
Quality control in pharmaceutical Industry
Quality Control in Pharmaceutical Industry
Quality Control in Pharmaceutical Industry
Prashant Tomar
G m p 01
G m p 01
saravanan vaidyanathan
for capsules and sterile products
Vendor Audit
Vendor Audit
PRAVADA
WHO Good Manufacturing Practice Requirements Good Manufacturing Practice is the part of quality assurance that ensures that products are consistently manufactured and controlled to the quality standards appropriate to their intended use.
WHO GMP Requirements
WHO GMP Requirements
Deekshitha HS
THIS PRESENTATION IS ABOUT THE CHANGE CONTROL IN PHARMACEUTICALS
CHANGE CONTROL
CHANGE CONTROL
sonia nazir
presentation on GMP training
Gmp change control by amsavel
Gmp change control by amsavel
Amsavel Vel
This presentation has been prepared from publicly available materials on the world wide web.
Product Quality Review (PQR)
Product Quality Review (PQR)
Rikul Patel
just for an idea
calulation of yields, production record review,change control
calulation of yields, production record review,change control
srikrupa institute of pharmaceutical analysis
TECHSHORE INSPECTION SERVICES|INSTITUTE OF QA/QC IN KERALA|ANTICIPATING CONSTRUCTION DEFECTS THROUGH EFFECTIVE QUALITY CONTROL
Qa qc course in Techshore inspection services
Qa qc course in Techshore inspection services
Techshore Inspection Services
Quality Assurance techniques
Emergent trends in QA of drug
Emergent trends in QA of drug
krushnakantwable
introduction About The Audits Of microbiological Laboretories
Auditing of microbiology laboratory
Auditing of microbiology laboratory
Nikita Amane
ICH Q10 guideline for pharmacutical industry.
ICH Q10
ICH Q10
Abu Naim Shekh
Tendances
(20)
Second Party Audit and External Third Party Audit
Second Party Audit and External Third Party Audit
Change control oos oot
Change control oos oot
Quality & GMP Presentation
Quality & GMP Presentation
2) Total Quality Managment
2) Total Quality Managment
Quality Systems Approach to Pharmaceutical cGMP
Quality Systems Approach to Pharmaceutical cGMP
Quality control grp.7 (49-56)
Quality control grp.7 (49-56)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Qc, qa
Qc, qa
Quality Control in Pharmaceutical Industry
Quality Control in Pharmaceutical Industry
G m p 01
G m p 01
Vendor Audit
Vendor Audit
WHO GMP Requirements
WHO GMP Requirements
CHANGE CONTROL
CHANGE CONTROL
Gmp change control by amsavel
Gmp change control by amsavel
Product Quality Review (PQR)
Product Quality Review (PQR)
calulation of yields, production record review,change control
calulation of yields, production record review,change control
Qa qc course in Techshore inspection services
Qa qc course in Techshore inspection services
Emergent trends in QA of drug
Emergent trends in QA of drug
Auditing of microbiology laboratory
Auditing of microbiology laboratory
ICH Q10
ICH Q10
En vedette
Responding To A 483and Warning Letter
Responding To A 483and Warning Letter
John E. Osani
PCrompton_Warning Letter Response
PCrompton_Warning Letter Response
Philip Crompton
Fda warning letter 3 5-2013 to dialysis drug maker and dialysis provider Fres...
Fda warning letter 3 5-2013 to dialysis drug maker and dialysis provider Fres...
Michael J. Evans
A mock response to a FDA warning letter
Mock Response to a FDA Warning Letter
Mock Response to a FDA Warning Letter
muna_ali
How to Sales & before Sale Selling your Self ! Steps of Sales , This presentation ideal to learn more and follow steps of selling. Your expert opinion will be highly beneficial in this regards.
Selling your self
Selling your self
Abdul Qadeer Qureshi
GPC-IR technology to deformulate complex polymer systems and to characterize copolymer compositional variations
GPC-IR To Charaterize Polymer Mixtures--Akron Workshop
GPC-IR To Charaterize Polymer Mixtures--Akron Workshop
mzhou45
READ MUST...
NAGARAJ GONI PRESENTATION ABOUT AUTO SUSPENTION.
NAGARAJ GONI PRESENTATION ABOUT AUTO SUSPENTION.
nagaraj goni
it is describe the various pharmaceutical companies in india
Pharmaceutical industry in india
Pharmaceutical industry in india
Somnath Surai
You receive a Warning Letter-- you have 15 days to submit a response. If FDA finds your response inadequate, you may receive a Consent Decree, which will cost millions to remediate. You need a process in place to react to a Warning Letter before it is delivered. These experts will discuss planning, procedures, training and ways to keep from getting a warning letter in the first place.
Responding Effectively to FDA 483 Observations & Warning Letters
Responding Effectively to FDA 483 Observations & Warning Letters
Maetrics
How to succeed when you get a FDA 483 form letter. What to do and how to handle your FDA 483. For more information go to http://compliance-insight.com/fda-483-warning-letters/fda-483-observations/
FDA 483
FDA 483
Compliance Insight, Inc.
Content: Introduction of Odoo Warehouse Management Understanding Double-Entry Stock Management Create Stock Locations Create products / components How to set opening stock Set minimum stock rules Stock Valuation
Odoo Warehouse
Odoo Warehouse
Matiar Rahman
A review on Production Planning and Control - Definitions of production, production planning, production control, production management, steps involved in production planning, steps involved in production control
PRODUCTION PLANNING AND CONTROL
PRODUCTION PLANNING AND CONTROL
Priyanka Modugu
How SYSPRO adds value to companies involved in pharmaceuticals.
Pharmaceuticals - Industry Value Chain
Pharmaceuticals - Industry Value Chain
SYSPRO
HPLC2010 Boston Presentation
HPLC2010 Pharmaceutical Copolymer Excipient Characterization By GPC-FTIR
HPLC2010 Pharmaceutical Copolymer Excipient Characterization By GPC-FTIR
mzhou45
plannin,production & control
production,planning and control
production,planning and control
Anil Kollur
The new Odoo warehouse management system
The new Odoo warehouse management system
Odoo
Quality control and quality assurance are vital in this industry. Many production workers are assigned full time to quality control and quality assurance functions, whereas other employees may devote part of their time to these functions. For example, although pharmaceutical company sales representatives, often called detailers, work primarily in marketing, they engage in quality control when they assist pharmacists in checking for outdated products. Advances in manufacturing processes are also impacting the industry. While pharmaceutical manufacturers have long devoted resources to new drug development as a source for future profits, firms are increasingly realizing that improvements throughout the drug pipeline are needed to stay competitive. See more http://goo.gl/1sQLwS http://goo.gl/jajeNa http://goo.gl/0tvlst http://www.entrepreneurindia.co/ Tags Pharmaceutical Technology Books, Essentials of Pharmaceutical Technology, Pharmaceutical Technology, Pharmaceutical books, Science, Technology & Medicine Books, Drugs technology books, Drug and Pharmaceuticals technology book, Best small and cottage scale industries, Bulk Drugs Formulation, Bulk Drugs Manufacturing Industry, Business consultancy, Business consultant, Business guidance for Pharmaceutical industry, Business guidance to clients, Business Plan for a Startup Business, Creating a Pharma Start-up, Drug formulation manual, Formulation of Antibiotics, Formulation of Paracetamol, Formulation of Tablets, Great Opportunity for Startup, How to Start a Medicines manufacturing business?, How to start a pharmaceutical company, How to Start a Pharmaceutical Product Business, How to Start a Pharmaceutical Production Business, How to start a pharmacy business, How to start a successful drugs making business, How to start Antibiotics manufacturing business, How to start drugs pharmaceutical business, How to start medicine business, How to Start Medicine Manufacturing Industry in India, How to start medicine manufacturing, How to start Paracetamol production business, How to Start Pharmaceutical Manufacturing Company in India, Invest to setup a pharmaceutical business, Manufacturing of medicinal products- Pharmaceutical industry, Medicine Manufacturing Industry, Medicines Making Small Business Manufacturing, Modern small and cottage scale industries, Most Profitable Bulk Drugs production Business Ideas, New small scale ideas in Pharmaceutical industry, Pharma Manufacturing, Pharmaceutical and Medicines production Business, Pharmaceutical Based Profitable Projects, Pharmaceutical Based Small Scale Industries Projects, Pharmaceutical Drug Formulation, Pharmaceutical Drug Manufacturing Business, Pharmaceutical formulation guidelines, Pharmaceutical formulation, Pharmaceutical industry in India, Pharmaceutical industry, Pharmaceutical manufacturing Industry in India, Pharmaceutical Manufacturing Industry, Pharmaceutical Projects,
Pharmaceutical, Bulk Drugs and Medicine Manufacturing Industry (Production, F...
Pharmaceutical, Bulk Drugs and Medicine Manufacturing Industry (Production, F...
Ajjay Kumar Gupta
clearly describes the fundamental requirements of cGMP
Gmp final 97 03
Gmp final 97 03
Dr. Raja Abhilash
(This is an extract from the lecture delivered by Shyamsunder Panchavati on 2nd September 2010 at Hyderabad) Human being lives in whirlpool of Industries. All the industries revolve around the living beings specially the human beings. One industry or profession that keeps the human being fit enough to wither the whirlpool and keeps the industry going is the Medical Profession. Hence the Medical Profession occupies the high pedestal in this world. View the abstract at http://capacitybuildingdevelopment.blogspot.com/2010/09/pharmaceutical-industry-overview_06.html
Pharma industry an overview
Pharma industry an overview
Shyamsunder Panchavati
Trend and Opportunity in Pharma Sector
Pharmaceutical Industry
Pharmaceutical Industry
Amit Roy
En vedette
(20)
Responding To A 483and Warning Letter
Responding To A 483and Warning Letter
PCrompton_Warning Letter Response
PCrompton_Warning Letter Response
Fda warning letter 3 5-2013 to dialysis drug maker and dialysis provider Fres...
Fda warning letter 3 5-2013 to dialysis drug maker and dialysis provider Fres...
Mock Response to a FDA Warning Letter
Mock Response to a FDA Warning Letter
Selling your self
Selling your self
GPC-IR To Charaterize Polymer Mixtures--Akron Workshop
GPC-IR To Charaterize Polymer Mixtures--Akron Workshop
NAGARAJ GONI PRESENTATION ABOUT AUTO SUSPENTION.
NAGARAJ GONI PRESENTATION ABOUT AUTO SUSPENTION.
Pharmaceutical industry in india
Pharmaceutical industry in india
Responding Effectively to FDA 483 Observations & Warning Letters
Responding Effectively to FDA 483 Observations & Warning Letters
FDA 483
FDA 483
Odoo Warehouse
Odoo Warehouse
PRODUCTION PLANNING AND CONTROL
PRODUCTION PLANNING AND CONTROL
Pharmaceuticals - Industry Value Chain
Pharmaceuticals - Industry Value Chain
HPLC2010 Pharmaceutical Copolymer Excipient Characterization By GPC-FTIR
HPLC2010 Pharmaceutical Copolymer Excipient Characterization By GPC-FTIR
production,planning and control
production,planning and control
The new Odoo warehouse management system
The new Odoo warehouse management system
Pharmaceutical, Bulk Drugs and Medicine Manufacturing Industry (Production, F...
Pharmaceutical, Bulk Drugs and Medicine Manufacturing Industry (Production, F...
Gmp final 97 03
Gmp final 97 03
Pharma industry an overview
Pharma industry an overview
Pharmaceutical Industry
Pharmaceutical Industry
Similaire à Excipient Auditing
23 April & 21 May 2017 Discussion Forum
ICHQ7 & Q11 (4 of 7)
ICHQ7 & Q11 (4 of 7)
Hubdar Ali
Presented at length on 23 April and 21 May 2017 at ICCBS, HEJ and Getz Pharma Auditorium, Karachi in a Discussion Forum of about 800 practicing university qualified professionals of various pharmaceutical manufacturing industries
ICH Q7 & Q11
ICH Q7 & Q11
Obaid Ali / Roohi B. Obaid
Good Manufacturing Practices For Quality Control
Good Manufacturing Practices For Quality Control
Good Manufacturing Practices For Quality Control
Dr Rajendra Patel
Current Good Manufacturing Practices (cGMPs) provide the necessary environmental and operating conditions for the production of high quality and safe foods. They are also the building blocks for GFSI-recognized food safety and quality standards, including SQF, BRC, FSSC 22000, and other global standard schemes. This webinar on cGMPs for GFSI was co-hosted with founder and partner of Food Industry Consulting, Sonia Akbarzadeh, on October 7 at 10:00am MDT. Sonia covers cGMP basics and how you can use them as building blocks for GFSI compliance. Specifically, you hear more about: -Setting up detailed programs and procedures – the 4 stages of cGMPs -Controlling hazards introduced by personnel, environment, and operations -Common prerequisite programs -Elevating the importance of cGMPs as a path to reach GFSI compliance
Intro to cGMPs: The Building Blocks for GFSI Compliance
Intro to cGMPs: The Building Blocks for GFSI Compliance
TraceGains
tQmlab® is the premier management system for GxP operations and for supporting regulatory submissions. It delivers transformational productivity for QA/QC labs supporting customised workflows for quality control of drugs, stability testing, product release testing and post-release quality testing.
PAT and QbD concepts in designing the LiMS and other Electronic systems in La...
PAT and QbD concepts in designing the LiMS and other Electronic systems in La...
balakrishna t
pilot plant is a small system which is operated to find out about the behavior of a process before using it on a large industrial scale. so, this presentation tries to illustrate its objective and significance to understand the methodologies of various pharmaceutical dosage forms.
Pilot plant scaleup
Pilot plant scaleup
OMKARTAMBEKAR
It'a a presentation on GMP prepared for the seminar at the college. Includes general basics of GMP with simple understanding.
Good Manufacturing Practices (GMP)- Purpose and Principles
Good Manufacturing Practices (GMP)- Purpose and Principles
Imran Malik
glp
02Good Laboratory Practice (GLP)(1).pptx
02Good Laboratory Practice (GLP)(1).pptx
hailemeskelteshome
Quality Assurance
Quality system gmp
Quality system gmp
aveekdatta7
Advanced Pharmaceutical Technology
Raw Material Validation
Raw Material Validation
Hiron Devnath
U.S.F.D.A. was the pioneer in the concept of process validation. Validation had proven to be an important tool for quality management of pharmaceutical according to ISO 9000:2000.
Pharmaceutical validation
Pharmaceutical validation
amol dighe
U.S.F.D.A. was the pioneer in the concept of process validation. Validation had proven to be an important tool for quality management of pharmaceutical according to ISO 9000:2000.
Pharmaceutical validation
Pharmaceutical validation
amol dighe
GMP quality assurance
GMP quality assurance
Tilahun Alemayehu
Tutorial for Discussion
Case Study 2 RSSMP 12 Aug 2018
Case Study 2 RSSMP 12 Aug 2018
Obaid Ali / Roohi B. Obaid
An Interactive Workshop with Pharmaceutical Professional Engineers
HVAC & Water in Pharmaceutical Mnaufacturing; From Theory to Application
HVAC & Water in Pharmaceutical Mnaufacturing; From Theory to Application
Obaid Ali / Roohi B. Obaid
This presentation has been prepared by " Drug Regulations" a not for profit organization from publicly available materials on the world wide web.
Product quality review
Product quality review
GMP EDUCATION : Not for Profit Organization
Gmp Guidelines
Gmp Guidelines by HCP
Gmp Guidelines by HCP
Atlantic Training, LLC.
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Malla Reddy College of Pharmacy
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
ceutics1315
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Malla Reddy College of Pharmacy
Similaire à Excipient Auditing
(20)
ICHQ7 & Q11 (4 of 7)
ICHQ7 & Q11 (4 of 7)
ICH Q7 & Q11
ICH Q7 & Q11
Good Manufacturing Practices For Quality Control
Good Manufacturing Practices For Quality Control
Intro to cGMPs: The Building Blocks for GFSI Compliance
Intro to cGMPs: The Building Blocks for GFSI Compliance
PAT and QbD concepts in designing the LiMS and other Electronic systems in La...
PAT and QbD concepts in designing the LiMS and other Electronic systems in La...
Pilot plant scaleup
Pilot plant scaleup
Good Manufacturing Practices (GMP)- Purpose and Principles
Good Manufacturing Practices (GMP)- Purpose and Principles
02Good Laboratory Practice (GLP)(1).pptx
02Good Laboratory Practice (GLP)(1).pptx
Quality system gmp
Quality system gmp
Raw Material Validation
Raw Material Validation
Pharmaceutical validation
Pharmaceutical validation
Pharmaceutical validation
Pharmaceutical validation
GMP quality assurance
GMP quality assurance
Case Study 2 RSSMP 12 Aug 2018
Case Study 2 RSSMP 12 Aug 2018
HVAC & Water in Pharmaceutical Mnaufacturing; From Theory to Application
HVAC & Water in Pharmaceutical Mnaufacturing; From Theory to Application
Product quality review
Product quality review
Gmp Guidelines by HCP
Gmp Guidelines by HCP
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Quality assuranceandregulatorycomplianceforpharmaceuticalproduct(4)
Excipient Auditing
1.
Implementing GMP Auditing
Practices for Excipient Suppliers July 30, 2001
2.
3.
4.
Where does GMP
start? Review the scenarios and identify the processing point at which GMP principles should be applied. State your reasons as to why you feel this is the appropriate point to apply GMP.
5.
Where does GMP
start? NaOH
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
Traceable During Lifecycle
Manufacture Distribution Pharm User Consumer
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
Télécharger maintenant