Established in 2005, Applied Biopharm Consultancy provide quality assurance and compliance services to the biopharmaceutical industry, specialising in the preparation of quality documents to support the development, characterisation and validation of biological and biotechnology products. We have authored and reviewed numerous documents including standard operating procedures, protocols and reports to support the late stage development, validation and production of biotherapeutics. Applied Biopharm Consultancy has prepared quality documents for commercial and clinical manufacturing facilities that have successfully undergone regulatory (FDA and MHRA) inspections and can advise on all aspects of GMP compliance and manufacturing process development. We look forward to developing additional partnerships with industry and academia. Contact us today to discuss your requirements.