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Our ref.:DRAAPGENEVA, 21 September 2015Annexes: 4 (available in English only)Subject:Regional Forum for Directors of National Meteorological and Hydrological
Services in Regional Association V (SouthWest
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What is dra-ap?
DRA-AP stands for Drug Regulatory Authority - Annual Plan, which is a report that outlines the planned activities and compliance measures for the year regarding drug regulation.
Who is required to file dra-ap?
Manufacturers, distributors, and any entity involved in the pharmaceutical supply chain are required to file the DRA-AP.
How to fill out dra-ap?
To fill out the DRA-AP, entities must provide detailed information on their drug-related activities, compliance status, and planned objectives for the year in the designated format issued by the regulatory authority.
What is the purpose of dra-ap?
The purpose of the DRA-AP is to ensure transparency in drug regulation, facilitate oversight, and help the regulatory authority monitor compliance and safety in the pharmaceutical sector.
What information must be reported on dra-ap?
Entities must report information regarding their operations, compliance with regulations, yearly objectives, and any changes in manufacturing or distribution practices.
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