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We are there for you even after "Day 105"

We support and generate chemical and pharmaceutical documentation together with relevant expert reports and forms in the CTD format (for Common Technical Document for medicinal products for human use) and NTA Vet format (for veterinary medicinal products). And on day 105, when a review indicating risks from the relevant authorizing body arrives, we will show you how to remedy and eliminate these risks keeping within the stipulated 30-day term, by integrating our interdisciplinary network. As the international EU market is the goal (with niche products for the smaller German market remaining the exception), registration and defect processing documents will be generated in English as is often called for nowadays.