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EUSWISSMED looks for partnerships and clients who need QPPV services on an interim or project basis. Our special expertise is in post-market authorization products als well as for clinical studies phase II-IV. Our services are according to EMA and FDA regulations, including documentation in a safety database or alternatively the client's infrastructure. We are focused on medium-sized pharmaceutical companies. We also offer services in medical devices, e. g. in certification. Our team, including pharmacists, medical officers and biochemists is ready to start projects short-term.

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