1.

What Is A Marketing Authorization Application?

Answer»

It is an application FILED with the relevant authority in the Europe (typically, the UK's MHRA or the EMA’s Committee for Medicinal Products for HUMAN Use (CHMP)) to market a drug or medicine.

As per UK’s MHRA-

  • Applications for NEW active substances are described as 'full applications'.
  • Applications for medicines containing EXISTING active substances are described as 'abbreviated’ or ‘abridged applications’.

It is an application filed with the relevant authority in the Europe (typically, the UK's MHRA or the EMA’s Committee for Medicinal Products for Human Use (CHMP)) to market a drug or medicine.

As per UK’s MHRA-


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