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A practical approach for pharmacies and life science companies Quality audits are a crucial time for pharmacies, pharmaceutical companies and life science entities. They are not just about demonstrating compliance with regulatory requirements or reference standards, but about verifying the effectiveness of internal processes and the soundness of the management system adopted. Structured and knowledgeable […]

What the MDR Regulation entails for manufacturers, importers and distributors in Switzerland “Compliance is not an administrative goal, but the foundation of trust in the market.” With the entry into force of Regulation (EU) 2017/745(MDR), the medical device industry has undergone one of the most profound regulatory changes in decades. For Swiss companies-manufacturers, importers, and

Introduction In Switzerland, the pharmacy is not only a point of dispensing medicines, but a true health care advice center. To ensure high standards of safety, efficiency and reliability, pharmacies must implement quality management systems (QMS ) that comply with federal and cantonal regulations. These systems provide a structured basis for ensuring that every process-from

Swissdamed – UDI Devices Module As of Aug. 18, 2025, Swissmedic activated the UDI Devices module in the Swissdamed database, allowing voluntary registration of medical devices, IVDs, and kit/process packs (SPPs).From July 1, 2026, however, registration will become mandatory for all products placed on the Swiss market.There is also a short transition period until December

Why participate? The life-sciences industry is constantly evolving, and staying up-to-date on regulations and market trends is crucial, especially for pharmacies. This free webinar, organized by Pharmanomos Sagl in collaboration with AFTI (on the occasion of its 40th anniversary), provides a clear and up-to-date overview of topics critical to your business. Main topics of the