ADRES have over 30 years of experience with the FDA and leading regulatory bodies around the globe. Providing scientific and regulatory affairs, QA, CMC services in the States, Europe, Brazil, India China and Israel – from R&D and early-stage startups to big pharma, we are highly experienced in a variety of pharmaceutical fields including vaccines, biologicals, cell therapies and ATMPs, botanical drugs, liposomes and medical devices, all in pursuit of treatment for an array of medical conditions.

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