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.,
02 1M/s.RA Chem Pharma Ltd
01 2Piribedil IH
01 1WC-0150
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-602003 Tamil Nadu, In...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm : R. S. No. 50/1, Mukteswarapuram (V), Jaggalahpet (M), Krishna -District- 521175,...
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PharmaCompass offers a list of Piribedil 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 Piribedil manufacturer or Piribedil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Piribedil manufacturer or Piribedil supplier.
PharmaCompass also assists you with knowing the Piribedil API Price utilized in the formulation of products. Piribedil API Price is not always fixed or binding as the Piribedil Price is obtained through a variety of data sources. The Piribedil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trivastan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trivastan, including repackagers and relabelers. The FDA regulates Trivastan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trivastan 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 Trivastan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trivastan supplier is an individual or a company that provides Trivastan active pharmaceutical ingredient (API) or Trivastan finished formulations upon request. The Trivastan suppliers may include Trivastan API manufacturers, exporters, distributors and traders.
click here to find a list of Trivastan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trivastan written confirmation (Trivastan WC) is an official document issued by a regulatory agency to a Trivastan manufacturer, verifying that the manufacturing facility of a Trivastan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Trivastan APIs or Trivastan finished pharmaceutical products to another nation, regulatory agencies frequently require a Trivastan WC (written confirmation) as part of the regulatory process.
click here to find a list of Trivastan suppliers with Written Confirmation (WC) on PharmaCompass.
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