Categories: quality & compliance

  • "How FMD affects labeling, marketing and communication of prescription drugs" is the title of Sigma's lecture in Gothenburg, Malmö and Stockholm.

    Sigma can help your company get ready for FMD

    All prescription drugs produced after 2019-02-09 must be provided with safety features. This is, a little simplified, the meaning of the new EU directive FMD or Falsified Medicines Directive, 2011/62 / EC.
    To know how companies can and should act for the introduction of the regulatory framework, Sigma is now helping companies by organizing lectures on FMD. Responsible for the lectures are speci

Enter your email address to follow Sigma Group

When you choose to create a user account and follow a newsroom your personal data will be used by us and the owner of the newsroom, for you to receive news and updates according to your subscription settings.

To learn more about this, please read our Privacy Policy, which applies to our use of your personal data, and our Privacy Policy for Contacts, which applies to the use of your personal data by the owner of the newsroom you follow.

Please note that our Terms of Use apply to all use of our services.

You can withdraw your consent at any time by unsubscribing or deleting your account.
Check your inbox

Email sent to __email__. Click the link there to follow Sigma Group.

Okay