Excellence in writing
We stand for customized and well-structured study documents for successful submission, effective study conduct, and reporting of study results.
20 years of experience in writing specific documents for clinical trials with drugs (IMP) and Medical Devices (IMD)
Resilient, committed and used dealing with challenges of complex study designs and international and multilingual trials
Well-established and fine-tuned team collaboration
Study documents, analysis results and study reports in time
We are a full-service CRO. We take this literally – whether you choose all or some of our service functions.
Gesellschaft für Beratung, Planung und Durchführung zur Entwicklung neuer pharmazeutischer Produkte mbH
+49 251 270 778 – 0
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