01 1M/s Gland Pharma Limited
01 1HEPARIN SODIUM EP
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 Heparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin, including repackagers and relabelers. The FDA regulates Heparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin 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 Heparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heparin supplier is an individual or a company that provides Heparin active pharmaceutical ingredient (API) or Heparin finished formulations upon request. The Heparin suppliers may include Heparin API manufacturers, exporters, distributors and traders.
click here to find a list of Heparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Heparin written confirmation (Heparin WC) is an official document issued by a regulatory agency to a Heparin manufacturer, verifying that the manufacturing facility of a Heparin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Heparin APIs or Heparin finished pharmaceutical products to another nation, regulatory agencies frequently require a Heparin WC (written confirmation) as part of the regulatory process.
click here to find a list of Heparin suppliers with Written Confirmation (WC) on PharmaCompass.
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