Barbara has over 35 years experience in global drug development in industry and an agency focused on clinical operations, clinical development, inspection readiness, GCP, medical affairs, drug safety, clinical dossier preparations, agency interactions including FDA, EMA, Canada, PMDA and integrations and change management after mergers and acquisitions. Her work included biologics, biosimilars and small molecules. She has a special interest in medical law and loves cooking, biking and her grandchildren.
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