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Participation by Expressing Opinions about Guideline for Bioequivalence Studies of Veterinary Preparations

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The guide was adopted by the European Medicines Agency (EMA) and addresses the requirements for designing, conducting and evaluating bioequivalence studies for veterinary pharmaceuticals that are often required when applying for the registration of a generic drug.

05/09/2021 - 10/10/2021
sfda.dm@sfda.gov.sa
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Participation by Expressing Opinions about Guideline for Bioequivalence Studies of Veterinary Preparations
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Food and Drug Authority - Health Sector
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Last Modified Date: 02/09/2021 - 10:07 AM Saudi Arabia Time

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