MANAGEMENT

Mr. Dziabo has over forty years’ experience in the Pharmaceutical and Medical Device industry working for Allergan, Medtronic, Natural Disinfection Technologies (NDT), and PrimaPharma, Inc. and as a Regulatory/CMC consultant for “start-ups” including Allegro Ophthalmics, Eterna Tear and Aeon.  Mr. Dziabo has a degree in Chemistry from Mansfield University of Pennsylvania and an MBA from Pepperdine University. His work experience runs the gamut from bench chemist, Quality Control chemist, research chemist, Manager, Director and VP of Product Development groups. He is the author or co-author on 23 US and International Patents and has acted as an expert witness in industry legal proceedings. As VP of Regulatory Affairs, Quality and Product Development at PrimaPharma, Inc, a San Diego CDMO, he had led projects for Big Pharma (Allergan, Alcon, Bausch & Lomb) and many small to medium sized companies as well as start-ups in many different applications including, peptides, enzymes, ant-inflammatory, anti-infective, glaucoma, sterile pre-filled syringes, aerosols, lyophilization and sterile/aseptic fill. 

Mr. Dziabo has written, submitted and obtained FDA approval for drugs, devices (CDRH) as well as 510k device applications. Mr. Dziabo has hosted FDA PAI and GMP inspections and made presentations to CDRH staff in support of NDA’s and other submissions.