01 1M/s Gland Pharma Limited
01 1Dalteparin Sodium (Ph. Eur) (Low Molecular Weight Heparin)
01 1WC-0399
01 1India
Dalteparin Sodium (Ph. Eur) (Low Molecular Weight Heparin)
Date of Issue : 2017-07-05
Valid Till : 2020-07-05
Written Confirmation Number : WC-0399
Address of the Firm : Sy. No. 143 to 148 150 and 151 Near Gandimaisamma Cross Roads, D.P Pally, Dundig...
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A Nadroparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nadroparin, including repackagers and relabelers. The FDA regulates Nadroparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nadroparin 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 Nadroparin supplier is an individual or a company that provides Nadroparin active pharmaceutical ingredient (API) or Nadroparin finished formulations upon request. The Nadroparin suppliers may include Nadroparin API manufacturers, exporters, distributors and traders.
click here to find a list of Nadroparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nadroparin written confirmation (Nadroparin WC) is an official document issued by a regulatory agency to a Nadroparin manufacturer, verifying that the manufacturing facility of a Nadroparin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nadroparin APIs or Nadroparin finished pharmaceutical products to another nation, regulatory agencies frequently require a Nadroparin WC (written confirmation) as part of the regulatory process.
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