Categories: quality & compliance

  • 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

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