Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 1SUPRIYA LIFESCIENCE LIMITED Mumbai IN
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01 1Mepyramine maleate
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01 1India
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01 1Valid
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : CEP 2015-122 - Rev 01
Status : Valid
Issue Date : 2024-11-19
Type : Chemical
Substance Number : 278
19
PharmaCompass offers a list of Pyrilamine Maleate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pyrilamine Maleate manufacturer or Pyrilamine Maleate supplier for your needs.
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A Prefrin A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prefrin A, including repackagers and relabelers. The FDA regulates Prefrin A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prefrin A 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 Prefrin A supplier is an individual or a company that provides Prefrin A active pharmaceutical ingredient (API) or Prefrin A finished formulations upon request. The Prefrin A suppliers may include Prefrin A API manufacturers, exporters, distributors and traders.
click here to find a list of Prefrin A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prefrin A CEP of the European Pharmacopoeia monograph is often referred to as a Prefrin A Certificate of Suitability (COS). The purpose of a Prefrin A CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prefrin A EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prefrin A to their clients by showing that a Prefrin A CEP has been issued for it. The manufacturer submits a Prefrin A CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prefrin A CEP holder for the record. Additionally, the data presented in the Prefrin A CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prefrin A DMF.
A Prefrin A CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prefrin A CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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