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Global Regulatory Consulting, Audits, Training, Submissions - Pharmaceuticals, Biotechnology, Medical Devices, Food, Clinical Trials, Life Science, Biopharmaceuticals, Cosmetics, Nutraceuticals, Chemical, Consumer Products
Regulatory consulting, compliance, training, audits, quality systems for pharmaceuticals, medical devices, biotechnology, life sciences, food & beverages, medical products, healthcare, biopharmaceuticals, dietary supplements, nutraceuticals, cosmetics, veterinary medicine, healthcare, clinical trials industries for compliance,audits, approvals, quality systems, QSIT, QSR, premarket approvals, new drug applications, NDA, abbreviated new drug applications ANDA, PMA, 510k, quality audits, ICH consultants, CTD, warning letters, FDA-483, CE Mark, premarket approval, regulatory guidance, cGMP, ISO 13485, quality assurance, design controls, part 11, computer validation, process validation, dossiers, good manufacturing practices, project management, China CFDA, warning letters, FDA-483, food labeling, expert witnesses, food labeling, expert witness, compliance, CE marking, CE mark, EMEA, IVDD, MDD, scientific reviews, technical reviews, feasibility studies, STED, Japan PAL, registered agent, US agent
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