Good Clinical Practice: Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise Reference; Volume 2, Guidance

Selected FDA GCP/Clinical Trial Guidance Documents Grouped by Topic: * FDA Overview and Orientation * Introduction to GCP * Part I: General * Part II: Institutional Review Boards (IRBs) and Informed Consent * Part III: Drugs and Biologics * Part IV: Medical Devices * Part V: Manufacturing Requirements for Investigational Products * Part VI: Electronic Data Reference Tools * Part VII: Combined Glossary and Index for all Quality Guidance Documents

• | Author: Mindy J. Allport-Settle
• | Publisher: Pharmalogika
• | Publication Date: Oct 03, 2010
• | Number of Pages: 752 pages
• | Binding: Paperback or Softback
• | ISBN-10: 0982147686
• | ISBN-13: 9780982147689