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Origo Enterprises provides pharmaceutical consultancy services focused on formulation development, analytical method development, regulatory strategy, bioavailability/bioequivalence study support, cGMP compliance audits, dossier preparation for US/EU markets (including ANDA/NDA filings), outsourcing of manufacturing/testing/clinical studies, and strategic advisory for pharma companies. Their expertise covers generic dosage forms including injectables, ophthalmic products, tablets/capsules/semi-solids/NDDS. They also offer guidance on regulatory submissions to agencies such as USFDA and EMA.
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