DEVELOPMENT OF FINISHED PHARMACEUTICAL PRODUCTS

 Development requirements specification for finished pharmaceutical dosage form  Development of normative documents (ND or pharmacopoeial monograph of an enterprise (PME)) for pharmacopoeia substances (PhS) and finished pharmaceutical products (FPP)  Reproduction of the developed inspection methods (ND or PME) at the Customer’s equipment  Pilot samples of FPP  Laboratory production regulations for FPP

Development of formulation and technology of modern, advanced technology and high performance finished pharmaceutical dosage forms of original drugs and generics