01 1M/s. Concord Biotech Ltd.,
01 1Teicoplanin EP
01 1WC-0111
01 1India
Date of Issue : 2019-09-23
Valid Till : 2022-07-02
Written Confirmation Number : WC-0111
Address of the Firm : Plot No. 1482-1486, Trasad Road, Dholka, Dist- Ahmedabad
79
PharmaCompass offers a list of Teicoplanin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Teicoplanin manufacturer or Teicoplanin supplier for your needs.
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A Teicoplanin A2-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teicoplanin A2-5, including repackagers and relabelers. The FDA regulates Teicoplanin A2-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teicoplanin A2-5 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 Teicoplanin A2-5 supplier is an individual or a company that provides Teicoplanin A2-5 active pharmaceutical ingredient (API) or Teicoplanin A2-5 finished formulations upon request. The Teicoplanin A2-5 suppliers may include Teicoplanin A2-5 API manufacturers, exporters, distributors and traders.
click here to find a list of Teicoplanin A2-5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Teicoplanin A2-5 written confirmation (Teicoplanin A2-5 WC) is an official document issued by a regulatory agency to a Teicoplanin A2-5 manufacturer, verifying that the manufacturing facility of a Teicoplanin A2-5 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Teicoplanin A2-5 APIs or Teicoplanin A2-5 finished pharmaceutical products to another nation, regulatory agencies frequently require a Teicoplanin A2-5 WC (written confirmation) as part of the regulatory process.
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