01 1M/s Gland Pharma Limited
01 1Enoxaparin Sodium Ph.Eur
01 1WC-0356
01 1India
Date of Issue : 2020-02-10
Valid Till : 2022-02-02
Written Confirmation Number : WC-0356
Address of the Firm : Block C, Phase-I Visakhapatnam Special Economic Zone, Andhra Pradesh, India
A Enoxaparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enoxaparin, including repackagers and relabelers. The FDA regulates Enoxaparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enoxaparin 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 Enoxaparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Enoxaparin supplier is an individual or a company that provides Enoxaparin active pharmaceutical ingredient (API) or Enoxaparin finished formulations upon request. The Enoxaparin suppliers may include Enoxaparin API manufacturers, exporters, distributors and traders.
click here to find a list of Enoxaparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Enoxaparin written confirmation (Enoxaparin WC) is an official document issued by a regulatory agency to a Enoxaparin manufacturer, verifying that the manufacturing facility of a Enoxaparin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Enoxaparin APIs or Enoxaparin finished pharmaceutical products to another nation, regulatory agencies frequently require a Enoxaparin WC (written confirmation) as part of the regulatory process.
click here to find a list of Enoxaparin suppliers with Written Confirmation (WC) on PharmaCompass.
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