SERATEC

Seratec registers DMFs of innovative or generic APIs to the US-FDA or EMEA on behalf of pharmaceutical laboratories, mainly US based. Seratec can handle highly potent APIs in accordance with cGMP (regularly inspected by the US-FDA) from the gr to the ton, from complex, even multi-steps, organic synthesis, essentially within the context of niche markets.Successfully, Seratec was appointed as

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