01 1M/s. Apitoria Pharma Private Limited
01 1Nirmatrelvir IH
01 1WC-0023
01 1India
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Survey no. 52,53,58,59,61 to 78,127&128, Pydibhimanvaram Village &Sy.No. 1,2,4t0...
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A PF07321332 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PF07321332, including repackagers and relabelers. The FDA regulates PF07321332 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PF07321332 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A PF07321332 supplier is an individual or a company that provides PF07321332 active pharmaceutical ingredient (API) or PF07321332 finished formulations upon request. The PF07321332 suppliers may include PF07321332 API manufacturers, exporters, distributors and traders.
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A PF07321332 written confirmation (PF07321332 WC) is an official document issued by a regulatory agency to a PF07321332 manufacturer, verifying that the manufacturing facility of a PF07321332 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting PF07321332 APIs or PF07321332 finished pharmaceutical products to another nation, regulatory agencies frequently require a PF07321332 WC (written confirmation) as part of the regulatory process.
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