GMP Compliance Adviser | Free Demo Access

The world's largest GMP knowledge portal! 

• The trial period is absolutely non-binding. 
• It ends automatically after 7 days. 

How the GMP Compliance Adviser supports you 

GMP in Practice 

The GMP Compliance Adviser covers a wide range of topics: in 21 chapters, you will find more than 5,000 pages of in-depth knowledge for your everyday GMP work.

Here you will find expert knowledge from practical experience and requirements from the authorities' perspective:

• Quality Management, Quality Risk Management & Quality Control
• Premises, Facilities & Media
• Qualification, Process Validation & Cleaning Validation
• Hygiene, Microbiology & Monitoring
• Production, Sterile Production & Packaging
• Storage & Transport
• Audits and Supplier Qualification & Inspections and Drug Safety
• Documentation
• Computerised Systems & Data Integrity
• Active Pharmaceutical Ingredients & Biotechnology

GMP Regulations 

All relevant national, European and international GMP regulations are available in the GMP Compliance Adviser. Our editorial team keeps track of changes and updates for you, so that you always have access to the latest versions: 

• EU GMP Guide & EU directives 
• Regulations for Germany, Switzerland and Austria 
• Regulations governing medical devices 
• FDA regulations and guidelines 
• Guidelines from ICH, PIC/S and WHO