Diapharm creates access.
Access to markets, products, consumers, and patients — locally, nationally, across Europe, and worldwide.
As a management consultancy firm, Diapharm supports the pharmaceutical and life sciences industries, creating market access and value with foresight and creativity for nearly 40 years.
Diapharm provides regulatory strategy, product development, market access, quality management, and medical affairs support for medicinal products, medical devices, diagnostics, food supplements, and cosmetics.
Global Market Access and Legal Responsibility
Diapharm makes it possible for international pharmaceutical companies to successfully enter the European market. As a legal manufacturer, we assume regulatory responsibility for medical devices in Europe and third countries. In the UK, we serve as an authorized representative. Worldwide, we audit active ingredient manufacturers.
Marketing Authorization Procedures and Pharmacovigilance in Europe
Diapharm manages national and European marketing authorization procedures — whether it’s centralized European Medicine Agency (EMA) procedures, decentralized across EU member states, or national. Under our manufacturing and import authorization, we handle EU import approvals for medicinal products and ensure compliance with European pharmacovigilance requirements by providing an EU QPPV (Qualified person responsible for pharmacovigilance).
Responsibility and Quality Management in the DACH region
In the DACH region, we assume roles such as the responsible person for wholesale (Germany), the national QPPV (Austria), and the person responsible for advertising (Switzerland). Diapharm understands the European directives and the resulting national laws and implements GMP/GVP/GDP-compliant quality management systems. In Switzerland, Diapharm acts as the Swiss authorized representative for medical devices.
are maintained by Diapharm today, supporting these clients reliably and with commitment.
Collaboration built on trust.
shape everyday life at Diapharm — across all areas of expertise and product segments.
Work that drives progress.
are currently held by Diapharm — in diverse roles such as QPPV, wholesale representative, QP, or legal manufacturer for medical devices.
Commitment that makes a difference.
Expertise meets entrepreneurial spirit — regulation as the basis for market success.
The dialogue began in 1988.
With pharmaceutical and healthcare client consulting and market interaction.
Since then, Diapharm has brought expertise, pragmatism, and creative thinking to every challenge — while applying an entrepreneurial mindset. National and international companies turn to us for efficient market access and intelligent positioning. Regulatory affairs is the common thread that runs through everything we do. And we believe that true value often arises from extraordinary challenges — if tackled wisely and creatively.
Challenges create value.
Comprehensive expertise in healthcare products.
Our foundation: deep expertise in regulatory affairs, market access, medical affairs, quality management, product development and business development — for medicinal products, medical devices, and all types of health-related products. Our consultants — scientists, pharmacists, and physicians — combine scientific insight with strategic thinking and practical creativity, working closely with clients throughout project implementation.
European network, with an international presence.
Knowledge, initiative, and communication as success factors.
The mandates are both European and international; Diapharm is represented in Germany, Austria, Great Britain, and Switzerland. Diapharm’s work thrives on knowledge, initiative, and communication — and includes regular exchange with associations, academia, politics, and the public.
The conviction: problems can only be solved by those who commit to solving them
From early on, Diapharm took on regulatory roles like Information Officer and Graduated Plan Officer. Initially, this was met with criticism, but later it became clear that it was a groundbreaking approach for the industry.
2007
A new field: quality of medicines begins with the active ingredient — GMP audits ensure this.
Early on, Diapharm recognized the need for global API qualification — blue inspection. They audited manufacturers and produced high-quality API audit reports.
Relationship focused. Competent.
At Diapharm, consulting is much more than methodological competence and expertise: it requires empathy, critical thinking, creativity — and the dedication to tackle tasks with full conviction.
Consulting means moving the needle. And that’s exactly what we do — with empathy, experience, and drive.
A role at Diapharm combines communication with clarity, reliability with empathy, and precision with pragmatism.
You think holistically, across disciplines, and in a results-oriented way? You’re good at analyzing, assessing and making decisions? You understand people — both clients and colleagues? You communicate with confidence — both in German and English?
Then you’ll find exactly the right role at Diapharm.