PAI Pharma
Marissa Mitchell, M.S., currently serves as the Regulatory Affairs Manager, CMC at PAI Pharma since June 2022. With extensive experience in regulatory affairs, Marissa has held various positions including Regulatory Affairs Manager at Strides Pharma Inc. and Senior Associate Regulatory Affairs, CMC at Edenbridge Pharmaceuticals, LLC. Previous roles include Manager Regulatory Affairs at GlaxoSmithKline Consumer Healthcare, Regulatory CMC Associate Manager at Novartis, and Regulatory Affairs Associate at Teva Pharmaceuticals, where responsibilities encompassed post-approval submissions and change control assessments. Marissa's early career included roles in pharmacovigilance and quality analysis at Celgene Corporation and Glenmark Therapeutics. Marissa earned a Master of Science in Regulatory Affairs for Medical Products from Northeastern University and a Bachelor of Arts from Montclair State University.
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PAI Pharma
PAI Pharma is the industry leader of high-quality, US-made liquid and unit-dose medications. For over 50 years, PAI Pharma has produced and distributed suspensions, oral solutions, elixirs, syrups, liquids, and semi-solids. To meet the unique needs of retail chains, independent pharmacies, hospitals, long-term care facilities, and government agencies, we offer standard bottle packaging and ready-to-dispense unit-dose cups. Our mission is to participate in the creation of healthier lives by exceeding the expectations of those we serve. We do this by being the ultimate partner of choice—consistently, reliably, affordably deliver the medication the patient needs, every time.