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"The GMP Compliance Adviser is an indispensable tool for everyone who works in the regulated pharmaceutical sector."
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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
Sample Documents
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
Target Group
Managers in
- quality assurance,
- production,
- quality control,
- development in the pharmaceutical industry
as well as department heads in supplier industries such as
- plant manufacturers,
- consultants,
- planning offices.
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