Fishfa Biogenics: Renowned Manufacturer, & Exporter of Tacrolimus & Mupirocin API.
01 1M/s Fishfa Biogenics
02 1M/s Bills Biotech Pvt. Ltd
03 1M/s. Concord Biotech Ltd.,
01 1Mupirocin (IP/EP/USP)
02 1Mupirocin EP
03 1Mupirocin USP/BP/EP
01 1WC-0111
02 1WC-0489
03 1WC-0529n
01 3India
Fishfa Biogenics: Renowned Manufacturer, & Exporter of Tacrolimus & Mupirocin API.
Date of Issue : 2022-06-13
Valid Till : 2025-06-12
Written Confirmation Number : WC-0529n
Address of the Firm : (A division of Fishfa Rubbers Limited), Survey no 43/2/2,47/2, 50/1/2, 50/2, Kuv...
Date of Issue : 2023-11-15
Valid Till : 2026-11-15
Written Confirmation Number : WC-0489
Address of the Firm : Plot No P-1, Biotech Park, G.I.D.C, Manjusar TA: Savli, Dist. Vadodara, Gujarat
Date of Issue : 2022-12-16
Valid Till : 2025-07-02
Written Confirmation Number : WC-0111
Address of the Firm : Survay No. 1482-1486,Trasad Road, Dholka, Dist:- Ahmedabad-382225, Gujarat
91
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A Spectroderm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Spectroderm, including repackagers and relabelers. The FDA regulates Spectroderm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Spectroderm 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 Spectroderm supplier is an individual or a company that provides Spectroderm active pharmaceutical ingredient (API) or Spectroderm finished formulations upon request. The Spectroderm suppliers may include Spectroderm API manufacturers, exporters, distributors and traders.
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A Spectroderm written confirmation (Spectroderm WC) is an official document issued by a regulatory agency to a Spectroderm manufacturer, verifying that the manufacturing facility of a Spectroderm active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Spectroderm APIs or Spectroderm finished pharmaceutical products to another nation, regulatory agencies frequently require a Spectroderm WC (written confirmation) as part of the regulatory process.
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