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 Liquemin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liquemin, including repackagers and relabelers. The FDA regulates Liquemin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liquemin 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 Liquemin supplier is an individual or a company that provides Liquemin active pharmaceutical ingredient (API) or Liquemin finished formulations upon request. The Liquemin suppliers may include Liquemin API manufacturers, exporters, distributors and traders.
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A Liquemin written confirmation (Liquemin WC) is an official document issued by a regulatory agency to a Liquemin manufacturer, verifying that the manufacturing facility of a Liquemin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Liquemin APIs or Liquemin finished pharmaceutical products to another nation, regulatory agencies frequently require a Liquemin WC (written confirmation) as part of the regulatory process.
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