EU GMP compliance services

• GMP-system implementation and upgrade
• Audit and inspection for ISO and CMP compliance – international
• Pharmaceutical procurement and supplier qualification
• DIN EN ISO 13485 and 9001 quality management system
• Process risk management and technical risk analysis
• Risk-based qualification of equipment, plant and production lines
• Validation of systems, methods and processes
• GMP logistics and Good Distribution Practice
• Cleanroom operation and technology
• Excipient/active pharmaceutical ingredient (API)
• Pharmaceutical aseptic manufacturing
• Process technology and pharmaceutical packaging
• GMP workshops and trainings

When it comes to achieving EU GMP compliance for your pharmaceutical production facility you cannot afford to take risks. As a manufacturer, you need a corresponding certification, which you can obtain by passing a MP inspection for your production facility. SERCOTEC will be your first choice EU GMP compliance partner. Even if you are still thinking about how you would like to market your product in the EU, we will be happy to assist you.
SERCOTECH supports you extensively with the implementation of the EU CMP guidelines. Thus, your focus can stay on your all-day work. Our experts are addressing professionally and efficiently our various and demanding OMP requirements. We are able to offer individual niche solutions for our challenges as well as comprehensive packages that cover all your GMP requirements. SERCOTEC offers a wide range of services in terms of Good Manufacturing Practice (GMP) compliance. Whether concerning GMP compliance, CMP consulting or execution of qualification and validation, we support you extensively with the implementation of your projects.
With us, you obtain your manufacturing authorization and the corresponding MP certificate within the shortest possible time and move your business idea forward as quicklv as possible.