GMP Compliance Adviser | Free Demo Access
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The world's largest GMP knowledge portal.
Includes AI-powered search with GMP Chat: Get quick and reliable answers to your specific GMP questions, directly based on the content of the GMP Compliance Adviser.
Try it now for free. The demo access is non-binding. No cancellation is required.
It ends automatically after 14 days.
Special Offer as Part of Your Free Demo Access:
Select one of the 21 chapters from the GMP in Practice section of the GMP Compliance Adviser—we’ll grant you full access to it until the end of your trial period.
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- You will receive your login credentials via email.
- Throughout the week, you will receive further information about GMP Compliance Adviser directly in your inbox.
- Customer support is available to assist you at any time.
- You can also direct questions about the content to the editorial team and receive personalized responses.
- You do not need to cancel your demo access. The free access will end automatically.
Special Offer as Part of Your Free Demo Access:
Select one of the 21 chapters from the GMP in Practice section of the GMP Compliance Adviser—we’ll grant you full access to it until the end of your trial period.
This allows you to delve deeply into the topic that’s most relevant to your daily practice.
Take this opportunity to experience the in-depth technical content, practical explanations, and comprehensive expert knowledge the GMP Compliance Adviser has to offer—and see the tangible added value it brings to your work.
How the GMP Compliance Adviser supports you
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
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
In addition, the GMP Compliance Adviser contains many sample documents and practical examples that you can use:
- Sample SOPs
- Sample protocols
- Sample forms
- Case studies
AI in the GMP Compliance Adviser
Your AI assistant GMP Chat supports you in your work in the GMP Compliance Adviser.
GMP Chat only accesses the verified knowledge of the GMP Compliance Adviser, so you receive well-founded, trustworthy answers, including sources.
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