Announcements

Medfiles can help you ensure the safety of your products according to new GVP Module VI requirements

From 22-November-2017 we will step into the new Guideline on good pharmacovigilance practices (GVP) - Module VI – Collection, management and submission of reports of suspected adverse reactions to medicinal products. Are you ready to manage the safety of your products according to new GVP Module VI?

More information here

  • 15.11.2017

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