EMA Guideline on the Chemistry of Active Substances

Active Substance

Are you preparing submissions to the EMA for marketing authorization this year?  This guideline goes into effect in July 2017 and describes the type of information required for the manufacture and control of active substances used in medicinal products for EMA marketing authorization. It replaces the “Note for guidance on chemistry of new active” (CPMP/QWP/130/96, Rev 1) and “Chemistry of active substances” (3AQ5a) and covers new and existing active substances in one guideline. 

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European Medicines Agency (EMA) Mutual Recognition Agreement (MRA)

The EMA and FDA have agreed to recognize each other’s GMP inspections.  This Mutual Recognition Agreement goes into effect on November 1, 2017 to allow each other to:

  • rely on each other’s GMP inspections;
  • waive any requirements for batch testing of products on entry into their territories, after a transition phase;
  • share information on inspection outcomes and quality defects.

    This means that FDA inspections in the EU or EU inspections in the USA should be only performed in exceptional cases.

Read more here.