01 1M/s Sionc Phamaceuticals Pvt Ltd
01 1Tretinoine USP
01 1WC-0273
01 1India
Date of Issue : 2020-07-23
Valid Till : 2023-05-11
Written Confirmation Number : WC-0273
Address of the Firm : Plot No. 34A, J.N.Pharma City, Thanam (V), Parawada (M), Vishakhapatnam-District...
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PharmaCompass offers a list of Tretinoin 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 Tretinoin manufacturer or Tretinoin supplier for your needs.
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PharmaCompass also assists you with knowing the Tretinoin API Price utilized in the formulation of products. Tretinoin API Price is not always fixed or binding as the Tretinoin Price is obtained through a variety of data sources. The Tretinoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AVITA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AVITA, including repackagers and relabelers. The FDA regulates AVITA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AVITA 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 AVITA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AVITA supplier is an individual or a company that provides AVITA active pharmaceutical ingredient (API) or AVITA finished formulations upon request. The AVITA suppliers may include AVITA API manufacturers, exporters, distributors and traders.
click here to find a list of AVITA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AVITA written confirmation (AVITA WC) is an official document issued by a regulatory agency to a AVITA manufacturer, verifying that the manufacturing facility of a AVITA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AVITA APIs or AVITA finished pharmaceutical products to another nation, regulatory agencies frequently require a AVITA WC (written confirmation) as part of the regulatory process.
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