Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1M/s Nuray Chemicals Pvt Ltd.,
01 1Trientine Tetrahydrochloride IH
01 1WC-0416
01 1India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
Trientine Tetrahydrochloride IH
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm : Plot No. 111 SIDCO Industrial Estate, Kakkalur Thiruvallur-602003 Tamil Nadu, In...
A Trientine Tetrahydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trientine Tetrahydrochloride, including repackagers and relabelers. The FDA regulates Trientine Tetrahydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trientine Tetrahydrochloride supplier is an individual or a company that provides Trientine Tetrahydrochloride active pharmaceutical ingredient (API) or Trientine Tetrahydrochloride finished formulations upon request. The Trientine Tetrahydrochloride suppliers may include Trientine Tetrahydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trientine Tetrahydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trientine Tetrahydrochloride written confirmation (Trientine Tetrahydrochloride WC) is an official document issued by a regulatory agency to a Trientine Tetrahydrochloride manufacturer, verifying that the manufacturing facility of a Trientine Tetrahydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Trientine Tetrahydrochloride APIs or Trientine Tetrahydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Trientine Tetrahydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Trientine Tetrahydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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