已经在美国FDA注册的药品公司，经常被其客户或供应商要求核准其美国FDA注册真实有效。

百思企业咨询可以协助贵司出具FDA证书，用于侧面证明其注册在美国FDA真实有效。FDA官方从不颁发任何证书。

Drug companies can file a Drug Master File (DMF) in eCTD format to FDA, in order to keep their processing, material and facility confidential to the public. With the submission of DMF, the drug companies can authorize others to reference this DMF to support others' New Drug Application (NDA) or Abbreviated New Drug Application (ANDA) without disclosing any information related to Intellectual property. RGLM consulting is proud to assist customers to prepare and submit DMF to FDA.