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 Private Limited
02 1M/s. Apitoria Pharma Private Limited
01 2Brivudine IH
01 1WC-0023
02 1WC-0416
01 2India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
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 602 003, Tamil Nadu...
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Survey no. 52,53,58,59,61 to 78,127&128, Pydibhimanvaram Village &Sy.No. 1,2,4t0...
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A (E)-5-(2-Bromovinyl)-deoxyuridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (E)-5-(2-Bromovinyl)-deoxyuridine, including repackagers and relabelers. The FDA regulates (E)-5-(2-Bromovinyl)-deoxyuridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (E)-5-(2-Bromovinyl)-deoxyuridine 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 (E)-5-(2-Bromovinyl)-deoxyuridine supplier is an individual or a company that provides (E)-5-(2-Bromovinyl)-deoxyuridine active pharmaceutical ingredient (API) or (E)-5-(2-Bromovinyl)-deoxyuridine finished formulations upon request. The (E)-5-(2-Bromovinyl)-deoxyuridine suppliers may include (E)-5-(2-Bromovinyl)-deoxyuridine API manufacturers, exporters, distributors and traders.
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A (E)-5-(2-Bromovinyl)-deoxyuridine written confirmation ((E)-5-(2-Bromovinyl)-deoxyuridine WC) is an official document issued by a regulatory agency to a (E)-5-(2-Bromovinyl)-deoxyuridine manufacturer, verifying that the manufacturing facility of a (E)-5-(2-Bromovinyl)-deoxyuridine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting (E)-5-(2-Bromovinyl)-deoxyuridine APIs or (E)-5-(2-Bromovinyl)-deoxyuridine finished pharmaceutical products to another nation, regulatory agencies frequently require a (E)-5-(2-Bromovinyl)-deoxyuridine WC (written confirmation) as part of the regulatory process.
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