ADRES Advanced Regulatory Services Ltd.

ADRES Advanced Regulatory Services Ltd. is rated 3 out of 5 in the category pharmaceuticals. Read and write reviews about ADRES Advanced Regulatory Services Ltd.. Confidently, smartly and effectively leading regulatory processes, we assist you in obtaining national and international approvals, expediting time to market. Products considered complex are our specialty. ADRES is a prominent, well-established regulatory and QA consulting company based in Rehovot, Israel. Established in 2009 by Ms. Rivka Zaibel with the mission of assisting Israeli biopharma companies in drug development processes, the company focuses on effective and lean regulatory and quality management strategies. ADRES has a superb reputation of assisting pharmaceutical companies in constructing their regulatory and scientific development strategies. In addition, ADRES has vast experience in providing QA consultancy and services to companies in GLP, GMP and GCP development stages. ADRES specialises in advanced and novel therapeutics for which regulation has not yet been established. The ADRES team is comprised of scientists and engineers as well as regulatory and quality experts. ADRES’ motto is to provide clients tailor-made solutions, with a smart and cost-effective approach to regulation and compliance. Our services include: Regulatory Affairs Quality Assurance / Compliance Medical QA Manufacturing and Controls (CMC) Data Integrity Project Management Services ADRES’ clients range from young start-up companies to commercial phase companies. Our clients operate 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. We provide services to clients around the globe including in Israel, the USA, Europe, Brazil, India and China. Our European subsidiary ADRES EU B.V. is located in Amsterdam, The Netherlands. ADRES EU also serves as the European Representative during the conduct of clinical trials for pharmaceuticals and medical devices, as well as the European Representative for CE-marked medical devices.