01 1M/s Polypeptide laboratories Pvt ltd
01 1Triptorelin IH
01 1WC-0047a3
01 1India
Date of Issue : 2020-01-28
Valid Till : 2022-06-27
Written Confirmation Number : WC-0047a3
Address of the Firm : K-28, MIDC, Anandnagar, Ambernath (E), Thane-421 506
A Moapar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Moapar, including repackagers and relabelers. The FDA regulates Moapar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Moapar API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Moapar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Moapar supplier is an individual or a company that provides Moapar active pharmaceutical ingredient (API) or Moapar finished formulations upon request. The Moapar suppliers may include Moapar API manufacturers, exporters, distributors and traders.
click here to find a list of Moapar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Moapar written confirmation (Moapar WC) is an official document issued by a regulatory agency to a Moapar manufacturer, verifying that the manufacturing facility of a Moapar active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Moapar APIs or Moapar finished pharmaceutical products to another nation, regulatory agencies frequently require a Moapar WC (written confirmation) as part of the regulatory process.
click here to find a list of Moapar suppliers with Written Confirmation (WC) on PharmaCompass.
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