01 1M/s. Embio Ltd.,
01 1Selegiline Hydrochloride USP/BP/EP
01 1WC-0046
01 1India
Selegiline Hydrochloride USP/BP/EP
Date of Issue : 2022-09-01
Valid Till : 2025-07-28
Written Confirmation Number : WC-0046
Address of the Firm : Plot No. E-21, E-22/1, MIDC, Mahad, Dist. Raigad-402 309, Maharashtra
61
PharmaCompass offers a list of Selegiline Hydrochloride 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
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A Jumex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Jumex, including repackagers and relabelers. The FDA regulates Jumex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Jumex 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 Jumex supplier is an individual or a company that provides Jumex active pharmaceutical ingredient (API) or Jumex finished formulations upon request. The Jumex suppliers may include Jumex API manufacturers, exporters, distributors and traders.
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A Jumex written confirmation (Jumex WC) is an official document issued by a regulatory agency to a Jumex manufacturer, verifying that the manufacturing facility of a Jumex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Jumex APIs or Jumex finished pharmaceutical products to another nation, regulatory agencies frequently require a Jumex WC (written confirmation) as part of the regulatory process.
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