Anyone who manufactures medicinal products within the meaning of § 2(1) or (2) no. 1 on a commercial or professional basis requires an authorization from the competent authority. The same applies to legal persons, associations and partnerships without legal capacity.
Highlight & annotate passagesYour 360° partner for pharma compliance
Audits, pharmacovigilance, procurement and knowledge – competently from a single source. For pharma, medical devices, food supplements and veterinary medicine.
Your services – digitally available anytime
Through our web application you book and manage audits, access pharmacovigilance data and use our knowledge bases – transparent and in real time.
- Book and manage audits online
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Search our database of available 3rd-party GxP audits – live and without registration.
More than 50 strong cooperation partners
As Germany's largest purchasing cooperation in the pharmaceutical sector, we negotiate framework agreements for you with a broad network of established partners.
Pharma Audit
High-quality 3rd-party GxP audits – conducted worldwide, digitally managed.
Learn morePharmacovigilance
Adverse event capture, signal management and PSURs for compliance and patient protection.
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Purchasing cooperation, benchmarking and supplier risk management – robust and data-driven.
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eLearning, LMS, Pharma Codex and template contracts – expertise from practice.
Learn moreFour areas, one partner
From GxP audits and drug safety to procurement and knowledge – coordinated, all from a single source.


