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Jun 01 2016, Poland Food and Drug Administration (hereinafter referred to as SPDA) issued GMP inspection certificate: Shenzhen Techdow pharmaceutical Co,.Ltd. Pharmaceutical production was considered to comply with GMP eu directive 2003/94 / EC required, Granted by the European GMP inspection. At Oct.2015 and Apr.2016, SPDA Inspection group Appointments by European regulators, processed site GMP inspection for API and injection production separately. Throughout the process, the specialist and reviewers carried out with strict, comprehensive, systematic by means of Field tour, Access to Information, debrief, sample survey for the inspection. During the inspection, the whole company to complete all tasks cooperated with inspection work actively. Finally, Inspection group considered that Techdow API and injection production in line with the requirements of the European GMP, and we passed the site inspection ...