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 Heparin sodium 1,000 units in dextrose 5% in plastic container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin sodium 1,000 units in dextrose 5% in plastic container, including repackagers and relabelers. The FDA regulates Heparin sodium 1,000 units in dextrose 5% in plastic container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin sodium 1,000 units in dextrose 5% in plastic container 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 Heparin sodium 1,000 units in dextrose 5% in plastic container supplier is an individual or a company that provides Heparin sodium 1,000 units in dextrose 5% in plastic container active pharmaceutical ingredient (API) or Heparin sodium 1,000 units in dextrose 5% in plastic container finished formulations upon request. The Heparin sodium 1,000 units in dextrose 5% in plastic container suppliers may include Heparin sodium 1,000 units in dextrose 5% in plastic container API manufacturers, exporters, distributors and traders.
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A Heparin sodium 1,000 units in dextrose 5% in plastic container written confirmation (Heparin sodium 1,000 units in dextrose 5% in plastic container WC) is an official document issued by a regulatory agency to a Heparin sodium 1,000 units in dextrose 5% in plastic container manufacturer, verifying that the manufacturing facility of a Heparin sodium 1,000 units in dextrose 5% in plastic container active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Heparin sodium 1,000 units in dextrose 5% in plastic container APIs or Heparin sodium 1,000 units in dextrose 5% in plastic container finished pharmaceutical products to another nation, regulatory agencies frequently require a Heparin sodium 1,000 units in dextrose 5% in plastic container WC (written confirmation) as part of the regulatory process.
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