Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 1M/s. Synnat Pharma Private Limited
02 1M/sBiological E Limited
01 1Noscapine BP/USP/JP/Ph. Eur.
02 1Noscapine Ph. Eur
01 1WC-0301
02 1WC-0446
01 2India
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Date of Issue : 2024-05-22
Valid Till : 2027-07-02
Written Confirmation Number : WC-0301
Address of the Firm : Plot No. 60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Anakapalli District...
Date of Issue : 2022-12-14
Valid Till : 2025-08-04
Written Confirmation Number : WC-0446
Address of the Firm : Plot No. 4, Sy. No. 542/P, Biotech Park, Phase II, Kolthur Village, Shameerpet M...
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A Tuscalman manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tuscalman, including repackagers and relabelers. The FDA regulates Tuscalman manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tuscalman 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 Tuscalman manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tuscalman supplier is an individual or a company that provides Tuscalman active pharmaceutical ingredient (API) or Tuscalman finished formulations upon request. The Tuscalman suppliers may include Tuscalman API manufacturers, exporters, distributors and traders.
click here to find a list of Tuscalman suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tuscalman written confirmation (Tuscalman WC) is an official document issued by a regulatory agency to a Tuscalman manufacturer, verifying that the manufacturing facility of a Tuscalman active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tuscalman APIs or Tuscalman finished pharmaceutical products to another nation, regulatory agencies frequently require a Tuscalman WC (written confirmation) as part of the regulatory process.
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