Dr. Geigert has over 35 years of CMC industrial experience and leadership in the biopharmaceutical industry.
Active Pharmaceutical Ingredient (API) & Drug Product Specifications – From Clinical Development to Market Approval
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
CMC Regulatory Compliance for Biopharmaceuticals, Biosimilars and Other Biologics
Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, Biosimilars, Post-Approval
QA-QC Strategy for Biopharmaceuticals and Biologics
Stability Programs for Determining Product Shelf Life – From Clinical Development to Market Approval
CfPIE Improves Website Experience for Life Science Training Attendees
CfPIE Announces New Regulatory Compliance Training Course for Compound Pharmacies
CfPIE Discusses Life Sciences Training Advancements at Regulatory Conferences
New CAPA Process Course for Medical Device Professionals
Partnership with the Society for Clinical Data Management
The Center for Professional Innovation and Education (CfPIE) provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site and certification programs.
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