SlideShare une entreprise Scribd logo

Good Clinical Practices (Final With Links)

•Télécharger en tant que PPT, PDF•
•
G
guesta8ff9d

Good Clinical Practices

FormationSanté & Médecine
1  sur  34
Introduction: Good Clinical Practices
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Who Can Be An Investigator?
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object]
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Rules of Good Clinical Practice ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
Test Your Knowledge ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object]
[object Object]
[object Object],[object Object]
[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object]
IRB Approval ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
CONSENT Subjects must be fully informed about the study. ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
ASSENT For Children ,[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],You may have other reporting responsibilities (e.g. study sponsor, funding agency, NIH, etc.). You should learn what these are prior to initiating the study.
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object]
Scenario ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
[object Object],[object Object]

Recommandé

Audit, inspection and monitoring in clinical trial by Ashish singh parihar
Audit, inspection and monitoring in clinical trial by Ashish singh pariharAudit, inspection and monitoring in clinical trial by Ashish singh parihar
Audit, inspection and monitoring in clinical trial by Ashish singh pariharDr. Ashish singh parihar
 
Essential Documents For the Conduct of Clinical Trial
Essential Documents For the Conduct of Clinical TrialEssential Documents For the Conduct of Clinical Trial
Essential Documents For the Conduct of Clinical TrialClinosolIndia
 
Essential Documents for the Conduct Of a Clinical Trial
Essential Documents for the Conduct Of a Clinical TrialEssential Documents for the Conduct Of a Clinical Trial
Essential Documents for the Conduct Of a Clinical TrialTuracoz Skill Development Program
 
Site & investigator selection
Site & investigator selectionSite & investigator selection
Site & investigator selectionMukesh Jaiswal
 
Monitoring plan and basic monitoring visits: everything that a cra needs to know
Monitoring plan and basic monitoring visits: everything that a cra needs to knowMonitoring plan and basic monitoring visits: everything that a cra needs to know
Monitoring plan and basic monitoring visits: everything that a cra needs to knowTrialJoin
 
Source Documents in Clinical Trials_part1
Source Documents in Clinical Trials_part1Source Documents in Clinical Trials_part1
Source Documents in Clinical Trials_part1Valentyna Korniyenko
 
Essential documents
Essential documentsEssential documents
Essential documentsRajeev Sahai
 
Investigator Site File (ISF) / Trial Master file in trial (TMF)
Investigator Site File (ISF) / Trial Master file in trial (TMF)Investigator Site File (ISF) / Trial Master file in trial (TMF)
Investigator Site File (ISF) / Trial Master file in trial (TMF)KiranRajput38
 

Recommandé

Audit, inspection and monitoring in clinical trial by Ashish singh parihar
Audit, inspection and monitoring in clinical trial by Ashish singh pariharAudit, inspection and monitoring in clinical trial by Ashish singh parihar
Audit, inspection and monitoring in clinical trial by Ashish singh pariharDr. Ashish singh parihar
 
Essential Documents For the Conduct of Clinical Trial
Essential Documents For the Conduct of Clinical TrialEssential Documents For the Conduct of Clinical Trial
Essential Documents For the Conduct of Clinical TrialClinosolIndia
 
Essential Documents for the Conduct Of a Clinical Trial
Essential Documents for the Conduct Of a Clinical TrialEssential Documents for the Conduct Of a Clinical Trial
Essential Documents for the Conduct Of a Clinical TrialTuracoz Skill Development Program
 
Site & investigator selection
Site & investigator selectionSite & investigator selection
Site & investigator selectionMukesh Jaiswal
 
Monitoring plan and basic monitoring visits: everything that a cra needs to know
Monitoring plan and basic monitoring visits: everything that a cra needs to knowMonitoring plan and basic monitoring visits: everything that a cra needs to know
Monitoring plan and basic monitoring visits: everything that a cra needs to knowTrialJoin
 
Source Documents in Clinical Trials_part1
Source Documents in Clinical Trials_part1Source Documents in Clinical Trials_part1
Source Documents in Clinical Trials_part1Valentyna Korniyenko
 
Essential documents
Essential documentsEssential documents
Essential documentsRajeev Sahai
 
Investigator Site File (ISF) / Trial Master file in trial (TMF)
Investigator Site File (ISF) / Trial Master file in trial (TMF)Investigator Site File (ISF) / Trial Master file in trial (TMF)
Investigator Site File (ISF) / Trial Master file in trial (TMF)KiranRajput38
 
Monitoring of clinical trials
Monitoring of clinical trialsMonitoring of clinical trials
Monitoring of clinical trialskattamurilakshmi
 
Clinical Trials Monitoring
Clinical Trials MonitoringClinical Trials Monitoring
Clinical Trials Monitoringbodekerk
 
ICH-GCP Introduction
ICH-GCP IntroductionICH-GCP Introduction
ICH-GCP IntroductionAnsuman Parida
 
Role & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinatorRole & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinatorRadhika Nagare
 
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator MOHAMMEDSALEEMJM
 
Monitoring and auditing in clinical trials
Monitoring and auditing in clinical trialsMonitoring and auditing in clinical trials
Monitoring and auditing in clinical trialsJyotsna Kapoor
 
Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2heba rashed
 
Source Documents Slide Share
Source Documents Slide ShareSource Documents Slide Share
Source Documents Slide ShareKiranRajput38
 
SAE resporting for case 005
SAE resporting for case 005SAE resporting for case 005
SAE resporting for case 005Dr. Ashish singh parihar
 
Manisha ppt
Manisha pptManisha ppt
Manisha pptmanisha verma
 
Clinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility AnalysisClinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility AnalysisYing Lu
 
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...SOCRA CCRP Certification
 
New ct rule 2019
New ct rule 2019New ct rule 2019
New ct rule 2019Clinical Research Program, Gujarat University
 
Clinical research ppt,
Clinical research ppt,Clinical research ppt,
Clinical research ppt,Malay Singh
 
Terms & Terminology in Clinical Research
Terms & Terminology in Clinical ResearchTerms & Terminology in Clinical Research
Terms & Terminology in Clinical ResearchPayal1301
 
Imp management at site (UA)
Imp management at site (UA)Imp management at site (UA)
Imp management at site (UA)Pshot
 
Safety reporting of a clinical trial
Safety reporting of a clinical trialSafety reporting of a clinical trial
Safety reporting of a clinical trialGOURIPRIYA L S
 
Ndct rule 2019 (manisha)
Ndct rule 2019 (manisha)Ndct rule 2019 (manisha)
Ndct rule 2019 (manisha)ManishaChauhan86
 
Clinical trial monitoring
Clinical trial monitoringClinical trial monitoring
Clinical trial monitoringDr. Ashish singh parihar
 
SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019Shweta Lal
 
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st yearPresentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st yearAnubhav Singh
 
Principle of good clinical practice
Principle of good clinical practicePrinciple of good clinical practice
Principle of good clinical practiceInternational Islamic University Malaysia
 

Contenu connexe

Tendances

Monitoring of clinical trials
Monitoring of clinical trialsMonitoring of clinical trials
Monitoring of clinical trialskattamurilakshmi
 
Clinical Trials Monitoring
Clinical Trials MonitoringClinical Trials Monitoring
Clinical Trials Monitoringbodekerk
 
Role & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinatorRole & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinatorRadhika Nagare
 
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator MOHAMMEDSALEEMJM
 
Monitoring and auditing in clinical trials
Monitoring and auditing in clinical trialsMonitoring and auditing in clinical trials
Monitoring and auditing in clinical trialsJyotsna Kapoor
 
Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2heba rashed
 
Source Documents Slide Share
Source Documents Slide ShareSource Documents Slide Share
Source Documents Slide ShareKiranRajput38
 
Clinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility AnalysisClinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility AnalysisYing Lu
 
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...SOCRA CCRP Certification
 
Clinical research ppt,
Clinical research ppt,Clinical research ppt,
Clinical research ppt,Malay Singh
 
Terms & Terminology in Clinical Research
Terms & Terminology in Clinical ResearchTerms & Terminology in Clinical Research
Terms & Terminology in Clinical ResearchPayal1301
 
Imp management at site (UA)
Imp management at site (UA)Imp management at site (UA)
Imp management at site (UA)Pshot
 
Safety reporting of a clinical trial
Safety reporting of a clinical trialSafety reporting of a clinical trial
Safety reporting of a clinical trialGOURIPRIYA L S
 
SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019Shweta Lal
 

Tendances (20)

Monitoring of clinical trials
Monitoring of clinical trialsMonitoring of clinical trials
Monitoring of clinical trials
 
Clinical Trials Monitoring
Clinical Trials MonitoringClinical Trials Monitoring
Clinical Trials Monitoring
 
ICH-GCP Introduction
ICH-GCP IntroductionICH-GCP Introduction
ICH-GCP Introduction
 
Role & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinatorRole & responsibilities of a clinical research coordinator
Role & responsibilities of a clinical research coordinator
 
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator
 
Monitoring and auditing in clinical trials
Monitoring and auditing in clinical trialsMonitoring and auditing in clinical trials
Monitoring and auditing in clinical trials
 
Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2Essential Documents of Clinical Trials_2
Essential Documents of Clinical Trials_2
 
Source Documents Slide Share
Source Documents Slide ShareSource Documents Slide Share
Source Documents Slide Share
 
SAE resporting for case 005
SAE resporting for case 005SAE resporting for case 005
SAE resporting for case 005
 
Manisha ppt
Manisha pptManisha ppt
Manisha ppt
 
Clinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility AnalysisClinical Trial Protocol Review for Study Feasibility Analysis
Clinical Trial Protocol Review for Study Feasibility Analysis
 
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / ...
 
New ct rule 2019
New ct rule 2019New ct rule 2019
New ct rule 2019
 
Clinical research ppt,
Clinical research ppt,Clinical research ppt,
Clinical research ppt,
 
Terms & Terminology in Clinical Research
Terms & Terminology in Clinical ResearchTerms & Terminology in Clinical Research
Terms & Terminology in Clinical Research
 
Imp management at site (UA)
Imp management at site (UA)Imp management at site (UA)
Imp management at site (UA)
 
Safety reporting of a clinical trial
Safety reporting of a clinical trialSafety reporting of a clinical trial
Safety reporting of a clinical trial
 
Ndct rule 2019 (manisha)
Ndct rule 2019 (manisha)Ndct rule 2019 (manisha)
Ndct rule 2019 (manisha)
 
Clinical trial monitoring
Clinical trial monitoringClinical trial monitoring
Clinical trial monitoring
 
SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019SAE REPORTING TIMELINE AND COMPENSATION 2019
SAE REPORTING TIMELINE AND COMPENSATION 2019
 

En vedette

Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st yearPresentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st yearAnubhav Singh
 
Good Clinical Practice By: Swapnil L. patil
Good Clinical Practice By: Swapnil L. patilGood Clinical Practice By: Swapnil L. patil
Good Clinical Practice By: Swapnil L. patilSwapnil Patil
 
Good clinical practices
Good clinical practicesGood clinical practices
Good clinical practicesDhruva Sharma
 
Good Clinical Practice
Good Clinical PracticeGood Clinical Practice
Good Clinical PracticeMed Bee
 
R&D and Good Clinical Practice (GCP) 011910
R&D and Good Clinical Practice (GCP) 011910R&D and Good Clinical Practice (GCP) 011910
R&D and Good Clinical Practice (GCP) 011910Myron Pyzyk
 
Assessing students in clinical practice
Assessing students in clinical practiceAssessing students in clinical practice
Assessing students in clinical practicesgray2
 
Recurrent miscarriage: how to manage
Recurrent miscarriage: how to manageRecurrent miscarriage: how to manage
Recurrent miscarriage: how to manageHesham Al-Inany
 
Complementary and alternative therapies for hyperlipidemia
Complementary and alternative therapies for hyperlipidemiaComplementary and alternative therapies for hyperlipidemia
Complementary and alternative therapies for hyperlipidemiaNaina Mohamed, PhD
 
Clinical Practice Guidelines
Clinical Practice GuidelinesClinical Practice Guidelines
Clinical Practice Guidelinesssompur
 
Good Clinical Practices
Good Clinical PracticesGood Clinical Practices
Good Clinical PracticesKarun Kumar
 
The Enigma of implantation
The Enigma of implantationThe Enigma of implantation
The Enigma of implantationPriya Bhave.
 
Assignment 2 brain sex experiment
Assignment 2 brain sex experimentAssignment 2 brain sex experiment
Assignment 2 brain sex experimentSteven Ten
 

En vedette (20)

Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st yearPresentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
Presentation on Good Clinical Practices (GCP) By Anubhav Singh m.pharm 1st year
 
Principle of good clinical practice
Principle of good clinical practicePrinciple of good clinical practice
Principle of good clinical practice
 
Good Clinical Practice - KSR
Good Clinical Practice - KSRGood Clinical Practice - KSR
Good Clinical Practice - KSR
 
Good Clinical Practice By: Swapnil L. patil
Good Clinical Practice By: Swapnil L. patilGood Clinical Practice By: Swapnil L. patil
Good Clinical Practice By: Swapnil L. patil
 
Good Clinical Practice
Good Clinical PracticeGood Clinical Practice
Good Clinical Practice
 
Good clinical practices
Good clinical practicesGood clinical practices
Good clinical practices
 
Good Clinical Practice
Good Clinical PracticeGood Clinical Practice
Good Clinical Practice
 
R&D and Good Clinical Practice (GCP) 011910
R&D and Good Clinical Practice (GCP) 011910R&D and Good Clinical Practice (GCP) 011910
R&D and Good Clinical Practice (GCP) 011910
 
Combining GCP & GLP
Combining GCP & GLPCombining GCP & GLP
Combining GCP & GLP
 
PROLUTEX THE NEW progesterone
PROLUTEX THE NEW progesteronePROLUTEX THE NEW progesterone
PROLUTEX THE NEW progesterone
 
Assessing students in clinical practice
Assessing students in clinical practiceAssessing students in clinical practice
Assessing students in clinical practice
 
IVMS-CV Pharmacology-Hyperlipidemia Agents
IVMS-CV Pharmacology-Hyperlipidemia AgentsIVMS-CV Pharmacology-Hyperlipidemia Agents
IVMS-CV Pharmacology-Hyperlipidemia Agents
 
Recurrent miscarriage: how to manage
Recurrent miscarriage: how to manageRecurrent miscarriage: how to manage
Recurrent miscarriage: how to manage
 
Complementary and alternative therapies for hyperlipidemia
Complementary and alternative therapies for hyperlipidemiaComplementary and alternative therapies for hyperlipidemia
Complementary and alternative therapies for hyperlipidemia
 
Clinical Practice Guidelines
Clinical Practice GuidelinesClinical Practice Guidelines
Clinical Practice Guidelines
 
Good Clinical Practices
Good Clinical PracticesGood Clinical Practices
Good Clinical Practices
 
The Enigma of implantation
The Enigma of implantationThe Enigma of implantation
The Enigma of implantation
 
Gcp 2013
Gcp 2013Gcp 2013
Gcp 2013
 
Ich gcp
Ich gcpIch gcp
Ich gcp
 
Assignment 2 brain sex experiment
Assignment 2 brain sex experimentAssignment 2 brain sex experiment
Assignment 2 brain sex experiment
 

Similaire à Good Clinical Practices (Final With Links)

Investigators Responsibilities
Investigators Responsibilities Investigators Responsibilities
Investigators Responsibilities ClinosolIndia
 
Ethical review process, mk sharma
Ethical review process, mk sharmaEthical review process, mk sharma
Ethical review process, mk sharmaSHARDA UNIVERSITY
 
Investigators Responsibilities during Clinical trials
Investigators Responsibilities during Clinical trialsInvestigators Responsibilities during Clinical trials
Investigators Responsibilities during Clinical trialsBHAVYARAJAN2
 
Clinical trial study team
Clinical trial study teamClinical trial study team
Clinical trial study teamManjuJhakhar
 
clinical trial start up activities lahar ppt 3.pptx
clinical trial start up activities lahar ppt 3.pptxclinical trial start up activities lahar ppt 3.pptx
clinical trial start up activities lahar ppt 3.pptxLahar Sambana
 
institutional review board and independent ethics committee
institutional review board and independent ethics committeeinstitutional review board and independent ethics committee
institutional review board and independent ethics committeeMOHAMMAD ASIM
 
4.1.2 investigator.pptx
4.1.2 investigator.pptx4.1.2 investigator.pptx
4.1.2 investigator.pptxSyedaErum5
 
Good laboratoty practise
Good laboratoty practise Good laboratoty practise
Good laboratoty practise SUJITHA MARY
 
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...MedicReS
 
Assignment on Regulatory Prespectives of Clinical Trials
Assignment on Regulatory Prespectives of Clinical TrialsAssignment on Regulatory Prespectives of Clinical Trials
Assignment on Regulatory Prespectives of Clinical TrialsDeepak Kumar
 
responsibility of an investigator
responsibility of an investigatorresponsibility of an investigator
responsibility of an investigatordrodo2002
 
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptxROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptxPraveen kumar S
 
Sponsor Responsibilities ppt
Sponsor Responsibilities pptSponsor Responsibilities ppt
Sponsor Responsibilities pptSantosh Zarkariya
 
Role and Responsiblities of Sponsor as per ICH GCP.pptx
Role and Responsiblities of Sponsor as per ICH GCP.pptxRole and Responsiblities of Sponsor as per ICH GCP.pptx
Role and Responsiblities of Sponsor as per ICH GCP.pptxsreesujithra
 
Role and responsibilities of investigators as per ich
Role and responsibilities of investigators as per ichRole and responsibilities of investigators as per ich
Role and responsibilities of investigators as per ichManiz Joshi
 

Similaire à Good Clinical Practices (Final With Links) (20)

Investigators Responsibilities
Investigators Responsibilities Investigators Responsibilities
Investigators Responsibilities
 
Ethical review process, mk sharma
Ethical review process, mk sharmaEthical review process, mk sharma
Ethical review process, mk sharma
 
Investigators Responsibilities during Clinical trials
Investigators Responsibilities during Clinical trialsInvestigators Responsibilities during Clinical trials
Investigators Responsibilities during Clinical trials
 
Clinical trial study team
Clinical trial study teamClinical trial study team
Clinical trial study team
 
clinical trial start up activities lahar ppt 3.pptx
clinical trial start up activities lahar ppt 3.pptxclinical trial start up activities lahar ppt 3.pptx
clinical trial start up activities lahar ppt 3.pptx
 
A.baldridge cra ii april2016
A.baldridge cra ii april2016A.baldridge cra ii april2016
A.baldridge cra ii april2016
 
Ich e6(r1)
Ich e6(r1)Ich e6(r1)
Ich e6(r1)
 
institutional review board and independent ethics committee
institutional review board and independent ethics committeeinstitutional review board and independent ethics committee
institutional review board and independent ethics committee
 
4.1.2 investigator.pptx
4.1.2 investigator.pptx4.1.2 investigator.pptx
4.1.2 investigator.pptx
 
Good laboratoty practise
Good laboratoty practise Good laboratoty practise
Good laboratoty practise
 
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...
FDA 2013 Clinical Investigator Training Course: Ensuring the Safety of Clini...
 
58541541-GCP-GMP
58541541-GCP-GMP58541541-GCP-GMP
58541541-GCP-GMP
 
Assignment on Regulatory Prespectives of Clinical Trials
Assignment on Regulatory Prespectives of Clinical TrialsAssignment on Regulatory Prespectives of Clinical Trials
Assignment on Regulatory Prespectives of Clinical Trials
 
responsibility of an investigator
responsibility of an investigatorresponsibility of an investigator
responsibility of an investigator
 
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptxROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx
ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx
 
IRB (1).pdf
IRB (1).pdfIRB (1).pdf
IRB (1).pdf
 
Sponsor Responsibilities ppt
Sponsor Responsibilities pptSponsor Responsibilities ppt
Sponsor Responsibilities ppt
 
A researcher's guide to understanding clinical trials part 2
A researcher's guide to understanding clinical trials part 2A researcher's guide to understanding clinical trials part 2
A researcher's guide to understanding clinical trials part 2
 
Role and Responsiblities of Sponsor as per ICH GCP.pptx
Role and Responsiblities of Sponsor as per ICH GCP.pptxRole and Responsiblities of Sponsor as per ICH GCP.pptx
Role and Responsiblities of Sponsor as per ICH GCP.pptx
 
Role and responsibilities of investigators as per ich
Role and responsibilities of investigators as per ichRole and responsibilities of investigators as per ich
Role and responsibilities of investigators as per ich
 

Dernier

Organic Name Reactions for the students and aspirants of Chemistry12th.pptx
Organic Name Reactions for the students and aspirants of Chemistry12th.pptxOrganic Name Reactions for the students and aspirants of Chemistry12th.pptx
Organic Name Reactions for the students and aspirants of Chemistry12th.pptxVS Mahajan Coaching Centre
 
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...EduSkills OECD
 
Hybridoma Technology ( Production , Purification , and Application )
Hybridoma Technology ( Production , Purification , and Application ) Hybridoma Technology ( Production , Purification , and Application )
Hybridoma Technology ( Production , Purification , and Application ) Sakshi Ghasle
 
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxSOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxiammrhaywood
 
Arihant handbook biology for class 11 .pdf
Arihant handbook biology for class 11 .pdfArihant handbook biology for class 11 .pdf
Arihant handbook biology for class 11 .pdfchloefrazer622
 
mini mental status format.docx
mini mental status format.docxmini mental status format.docx
mini mental status format.docxPoojaSen20
 
Accessible design: Minimum effort, maximum impact
Accessible design: Minimum effort, maximum impactAccessible design: Minimum effort, maximum impact
Accessible design: Minimum effort, maximum impactdawncurless
 
Introduction to AI in Higher Education_draft.pptx
Introduction to AI in Higher Education_draft.pptxIntroduction to AI in Higher Education_draft.pptx
Introduction to AI in Higher Education_draft.pptxpboyjonauth
 
Measures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeMeasures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeThiyagu K
 
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17Incoming and Outgoing Shipments in 1 STEP Using Odoo 17
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17Celine George
 
The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13Steve Thomason
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfsanyamsingh5019
 
MENTAL STATUS EXAMINATION format.docx
MENTAL STATUS EXAMINATION format.docxMENTAL STATUS EXAMINATION format.docx
MENTAL STATUS EXAMINATION format.docxPoojaSen20
 
The basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxThe basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxheathfieldcps1
 
Concept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfConcept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfUmakantAnnand
 
Q4-W6-Restating Informational Text Grade 3
Q4-W6-Restating Informational Text Grade 3Q4-W6-Restating Informational Text Grade 3
Q4-W6-Restating Informational Text Grade 3JemimahLaneBuaron
 
APM Welcome, APM North West Network Conference, Synergies Across Sectors
APM Welcome, APM North West Network Conference, Synergies Across SectorsAPM Welcome, APM North West Network Conference, Synergies Across Sectors
APM Welcome, APM North West Network Conference, Synergies Across SectorsAssociation for Project Management
 

Dernier (20)

Organic Name Reactions for the students and aspirants of Chemistry12th.pptx
Organic Name Reactions for the students and aspirants of Chemistry12th.pptxOrganic Name Reactions for the students and aspirants of Chemistry12th.pptx
Organic Name Reactions for the students and aspirants of Chemistry12th.pptx
 
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
Presentation by Andreas Schleicher Tackling the School Absenteeism Crisis 30 ...
 
Hybridoma Technology ( Production , Purification , and Application )
Hybridoma Technology ( Production , Purification , and Application ) Hybridoma Technology ( Production , Purification , and Application )
Hybridoma Technology ( Production , Purification , and Application )
 
Staff of Color (SOC) Retention Efforts DDSD
Staff of Color (SOC) Retention Efforts DDSDStaff of Color (SOC) Retention Efforts DDSD
Staff of Color (SOC) Retention Efforts DDSD
 
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptxSOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
SOCIAL AND HISTORICAL CONTEXT - LFTVD.pptx
 
Arihant handbook biology for class 11 .pdf
Arihant handbook biology for class 11 .pdfArihant handbook biology for class 11 .pdf
Arihant handbook biology for class 11 .pdf
 
mini mental status format.docx
mini mental status format.docxmini mental status format.docx
mini mental status format.docx
 
TataKelola dan KamSiber Kecerdasan Buatan v022.pdf
TataKelola dan KamSiber Kecerdasan Buatan v022.pdfTataKelola dan KamSiber Kecerdasan Buatan v022.pdf
TataKelola dan KamSiber Kecerdasan Buatan v022.pdf
 
Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Bikash Puri Delhi reach out to us at 🔝9953056974🔝
 
Accessible design: Minimum effort, maximum impact
Accessible design: Minimum effort, maximum impactAccessible design: Minimum effort, maximum impact
Accessible design: Minimum effort, maximum impact
 
Introduction to AI in Higher Education_draft.pptx
Introduction to AI in Higher Education_draft.pptxIntroduction to AI in Higher Education_draft.pptx
Introduction to AI in Higher Education_draft.pptx
 
Measures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and ModeMeasures of Central Tendency: Mean, Median and Mode
Measures of Central Tendency: Mean, Median and Mode
 
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17Incoming and Outgoing Shipments in 1 STEP Using Odoo 17
Incoming and Outgoing Shipments in 1 STEP Using Odoo 17
 
The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdf
 
MENTAL STATUS EXAMINATION format.docx
MENTAL STATUS EXAMINATION format.docxMENTAL STATUS EXAMINATION format.docx
MENTAL STATUS EXAMINATION format.docx
 
The basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptxThe basics of sentences session 2pptx copy.pptx
The basics of sentences session 2pptx copy.pptx
 
Concept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.CompdfConcept of Vouching. B.Com(Hons) /B.Compdf
Concept of Vouching. B.Com(Hons) /B.Compdf
 
Q4-W6-Restating Informational Text Grade 3
Q4-W6-Restating Informational Text Grade 3Q4-W6-Restating Informational Text Grade 3
Q4-W6-Restating Informational Text Grade 3
 
APM Welcome, APM North West Network Conference, Synergies Across Sectors
APM Welcome, APM North West Network Conference, Synergies Across SectorsAPM Welcome, APM North West Network Conference, Synergies Across Sectors
APM Welcome, APM North West Network Conference, Synergies Across Sectors
 

Good Clinical Practices (Final With Links)

  • 1. Introduction: Good Clinical Practices
  • 2.
  • 3. Who Can Be An Investigator?
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.