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Post-authorization activities

Sopharma AD has an established medical governance unit with focus on post-authorization product information management.

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Led by industry Code of conduct we have developed adequate processes and procedures to ensure our promotional practices are ethical and lawful. Providing accurate and complete information to

  • physicians,
  • pharmacists and
  • other healthcare professionals

is our commitment.  

Sopharma AD takes responsibility to gather additional information about a medicine's safety, efficacy and optimal use after the regulatory approval. For its branded products the company performs post-authorization studies, published on the web site of the European clinical trials data base.