Our pharmacy experts
Producing, storing and administering IMP drugs safely requires deep GMP expertise and proven experience.
Our GMP facility is staffed by a dedicated team of experienced clinical trial pharmacists and QPs, all highly trained in the unique demands of phase I trials. We operate with a team of ten full-time licensed pharmacists, all trained in GMP, regularly re-evaluated and re-certified every two years. Our operation is built for reliability, flexibility and precision – ensuring that your IMPs are handled by professionals who fully understand the critical nature of early-phase development. This in-house capacity allows us to maintain full control over the production cycle – eliminating dependency on external hospital pharmacies or third-party providers.
We blend strict GMP compliance with the practical know-how to handle tight timelines, unstable formulations and unexpected challenges. HEAD OF PRODUCTION FACILITY AND QP, SGS ELLEN VERHAVERT ”
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