Compliance
Compliance with relevant and updated GxP law texts and norms plays an increasingly important role in the adjustment of quality and cost ...
Globalised markets mean new challenges.
Let’s face them together.
As a company in the field of life sciences, you need strong partners. The number of regulatory requirements both at home and abroad is constantly increasing. With us at your side, you will be ready for your ever more complex responsibilities. Thanks to our experience and our expertise, your processes and products will always be at the cutting edge of technology. Our services have a modular structure, are tailored to your requirements and uncompromisingly geared to quality. This website tells you more about us and our services.
We work with developers, manufacturers and distributors of medicines, medical devices, chemical active substances and biotech products. The work covers GxP compliance, gap analysis, interim roles, inspection readiness and training for your teams.
Gap analysis
What will the future bring? And are you prepared for any possible scenario? A gap analysis enables us to recognise possible strategic or operative gaps ...
Interim functions
If you require on-site support for a limited period of time, we will be available to you. We have taken on a wide variety of functions directly inside companies in ...
Audits
Before an FDA, WHO or ANVISA inspection, and before a licence or technology transfer, we review your company from the outside.
Trainings
We train teams in GxP, develop auditors and support sterile manufacturing and biotech production.