EssPhar Pvt Ltd

Business verticals for collaboration: • Formulation research and development & Technology Transfer (GENERIC; NDDS BASED GENERIC AND NEW PRODUCT DEVELOPMENT) • We are looking for MA holder for the dossier development and supply agreement from our associated contract manufacturing sites (accreditation with EU GMP / WHO GMP) at the best competitive prices and further out-licensing possibilities in different territories. • Looking for a MA holder who is specifically willing to develop the dossier of any old drug or BCS class I category where the additional expenses of bioequivalence studied can be a waiver, a comprehensive justification of making this approach will be supported with the dossier. • Sourcing of the pharmaceutical products in customer brands and labels at the best competitive prices from EU GMP approved / WHO GMP sites. • Supply of UK un-licensed products at the best price from EU-GMP approved sites. • Execution of site variation projects for EU-GMP certified pharmaceutical manufacturing sites • Pharmaceutical Site Manufacturing Projects for all dosage forms. • Analytical Method Development and Validation & Dossier Preparation. • We are engaged in manufacturing and commercializing pharmaceutical products worldwide. We supply all the dosage forms, oral solids, oral liquid, injectable, and topical products, with high quality at a reasonable price. We provide the products from EU GMP/TGA/HCA/other goods manufacturing compliance agencies, certified manufacturing sites.