Table of contents of journal:

Results: 9

Introduction to the clinical development process

Authors: Hamrell, MR

Citation: Mr. Hamrell, Introduction to the clinical development process, DRUG PHARM, 104, 2000, pp. 1-9

Statutory requirements and regulatory guidance

Authors: Woodrum, T Lee, DB Wallace, JR

Citation: T. Woodrum et al., Statutory requirements and regulatory guidance, DRUG PHARM, 104, 2000, pp. 11-37

Source documentation - Clinical auditors' observations

Authors: Molloy, VJ Mackintosh, DR

Citation: Vj. Molloy et Dr. Mackintosh, Source documentation - Clinical auditors' observations, DRUG PHARM, 104, 2000, pp. 39-47

Quality assurance in clinical trials

Authors: Kiernan, R

Citation: R. Kiernan, Quality assurance in clinical trials, DRUG PHARM, 104, 2000, pp. 49-62

Standardizing quality in international studies

Authors: Korteweg, M

Citation: M. Korteweg, Standardizing quality in international studies, DRUG PHARM, 104, 2000, pp. 63-97

Good clinical practices and computers

Authors: Woodrum, T

Citation: T. Woodrum, Good clinical practices and computers, DRUG PHARM, 104, 2000, pp. 99-108

Food and drug administration audit

Authors: Horowitz, AM

Citation: Am. Horowitz, Food and drug administration audit, DRUG PHARM, 104, 2000, pp. 109-125

GCP compliance assessed by independent auditing international similaritiesand differences

Authors: Bohaychuk, W Ball, G

Citation: W. Bohaychuk et G. Ball, GCP compliance assessed by independent auditing international similaritiesand differences, DRUG PHARM, 104, 2000, pp. 127-174

Fraud and misconduct in clinical research

Authors: Wells, F

Citation: F. Wells, Fraud and misconduct in clinical research, DRUG PHARM, 104, 2000, pp. 175-185

Risultati: 1-9 |