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      DMF overseas registration of pharmaceuticals DMF domestic registration of pharmaceuticals GMP compliance audit
      Position:Home > Regulatory services > GMP compliance audit

      Dragonpharm regulatory service introduction


      GMP compliance audit

      The entire pharmaceutical industry has continuously improved the requirements of the GMP regulations. Our regulatory team is committed to helping domestic pharmaceutical companies meet the requirements of GMP regulations and has participated in official audits and customer audits in various countries, including the European EDQM on-site audit and the Japanese PMDA on-site audit. , Brazil's official ANVISA audit, South Korea's official MFDS audit, Mexico's official audit, etc., the frequency of customer audits is countless, including many international pharmaceutical companies, such as MYLAN, TEVA, SANDOZ and so on.

      At the same time, we can also help foreign customers conduct third-party GMP audits, help customers choose the right suppliers, and confirm suppliers' GMP compliance status.

      Follow us
      Room No.:1001, Huahong Mansion No.1 Building 238 Tianmushan Road,Hangzhou, China E-mail:commercial@dragonpharm.com.cn Tel:86-571-85899500
      Hangzhou Dragonpharm Co., Ltd. Copyright(C)2018 Support by?chinachemnet?Chemnet?Toocle?Notice?