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21 CFR Part 211 Current Good Manufacturing Practice
Short Title:
21 CFR Part 210/211
Origin/Publisher:
FDA, USA, Center for Drug Evaluation and Research http://www.fda.gov/cder/dmpq/cgmpregs.htm
Document Type:
Code of Federal Regulations
Content:
Fundamental American GMP regulations for pharmaceutical manufacturers
GMP Conferences by Topics
- Quality Assurance
- GMP in Biotechnology
- Microbiology
- Regulatory Affairs
- GMP in Pharmaceutical Development
- Quality Control
- GDP
- Sterile / Aseptic Manufacturing
- Computer Validation
- Validation
- Technical Operations
- GMP for APIs and Excipients
- Medical Devices
- GMP Basic Training Courses
- Packaging
- Data Integrity