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BESTSELLER

1. GDP Audit Checklist
for the Storage and Transport of Pharmaceuticals

 

2. GMP Audit Checklist
for Pharmaceutical and API Manufacturers

 

3. Computer System Validation in the EU
a step-by-step guide to implementing a computer validation program

 

4. Risk Management
established methods of risk analysis
incl. ICH Q9

 

5. Preparing for the EU GMP Inspection
similarities - and subtle differences - between FDA and EU GMP inspections

 

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GMP MANUAL

GMP in Practice: 24 chapters written by internationally renowned industry experts.

 

GMP Regulations: 8 chapters with the most important GMP guidelines and regulations.

 

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