<code id="f8ygt"><small id="f8ygt"><track id="f8ygt"></track></small></code>

  • <center id="f8ygt"><small id="f8ygt"></small></center>

    1. <big id="f8ygt"></big>
      <big id="f8ygt"></big><code id="f8ygt"><nobr id="f8ygt"></nobr></code>
      <big id="f8ygt"></big>
    2. <center id="f8ygt"><em id="f8ygt"></em></center>
      DMF overseas registration of pharmaceuticals DMF domestic registration of pharmaceuticals GMP compliance audit
      REGULATORY SERVICES
      Position:Home > Regulatory services > DMF overseas registration of pharmaceuticals

      Dragonpharm regulatory service introduction

       

      DMF overseas registration of pharmaceuticals

      Our regulatory services team has a wealth of experience in overseas registration and has successfully assisted many pharmaceutical companies in China in registering EU EDMF files, applying for EU CEP, registration with Japan's JMF, registration with Russia's CIS, registration with other countries in Asia, and registration with South America (Brazil , Argentina, Intellect, Colombia, Mexico), Indian Registration, Middle East Registration (Egypt, Iran, Iraq, Jordan, Algeria) etc.

      With the implementation of eCTD, we can also help pharmaceutical companies edit and submit eCTD.

       

       

       

       

      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?
      久操伊人,91久久国产