Product Registration

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Highly qualified and continuously educated experts combine knowledge of scientific and regulatory aspects in order to compile new product dossiers of the highest quality in ECTD format. Our growing team always keeps abreast of international legislation, guidelines, regulatory requirements and customer needs, ensuring full compliance of the company’s products and practices. Specifar’s Regulatory team also advises on and co-ordinates the registration, approval and post-approval procedures of our pharmaceutical products world-wide. Our expertise in technical, clinical and registration issues ensures the most efficient and flexible approval procedures for Specifar and its partners.

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