$25 MAURITIUS RODRIGUEZ ISLAND (PP2301BB) KGV 10C SG 216 CANCEL SCARCE VFU Stamps British Colonies Territories Mauritius MAURITIUS RODRIGUEZ ISLAND PP2301BB KGV 未使用品 10C SG 216 CANCEL VFU SCARCE $25,ssgas.ru,216,RODRIGUEZ,SG,/microcellular1272502.html,KGV,SCARCE,10C,CANCEL,Stamps , British Colonies Territories , Mauritius,(PP2301BB),MAURITIUS,VFU,ISLAND $25 MAURITIUS RODRIGUEZ ISLAND (PP2301BB) KGV 10C SG 216 CANCEL SCARCE VFU Stamps British Colonies Territories Mauritius $25,ssgas.ru,216,RODRIGUEZ,SG,/microcellular1272502.html,KGV,SCARCE,10C,CANCEL,Stamps , British Colonies Territories , Mauritius,(PP2301BB),MAURITIUS,VFU,ISLAND MAURITIUS RODRIGUEZ ISLAND PP2301BB KGV 未使用品 10C SG 216 CANCEL VFU SCARCE

MAURITIUS 販売 RODRIGUEZ ISLAND PP2301BB KGV 未使用品 10C SG 216 CANCEL VFU SCARCE

MAURITIUS RODRIGUEZ ISLAND (PP2301BB) KGV 10C SG 216 CANCEL SCARCE VFU

$25

MAURITIUS RODRIGUEZ ISLAND (PP2301BB) KGV 10C SG 216 CANCEL SCARCE VFU

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Item specifics

Topic:
RODRIGUEZ ISLAND
Certification:
Uncertified
Quality:
Used
Grade:
VF (Very Fine)
Era:
George V (1910-1936)
Place of Origin:
Mauritius

MAURITIUS RODRIGUEZ ISLAND (PP2301BB) KGV 10C SG 216 CANCEL SCARCE VFU

International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use.

A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing, conducting, recording and reporting trials that involve participation of human subjects to ensure that the rights, safety and wellbeing of the trial subjects are protected. Ensure the credibility of clinical trial data.

TABLE OF CONTENTS

INTRODUCTION TO ICH GCP 

1. GLOSSARY 

2. THE PRINCIPLES OF ICH GCP 

3. INSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC) 

4. INVESTIGATOR 

5. SPONSOR 

6. CLINICAL TRIAL PROTOCOL AND PROTOCOL AMENDMENT(S) 

7. INVESTIGATOR’S BROCHURE 

8. ESSENTIAL DOCUMENTS FOR THE CONDUCT OF A CLINICAL TRIAL 

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