01 1M/s Maharshi Pharmachem Pvt ltd
01 1Diflucortolone Valerate BP
01 1WC-0485
01 1India
Date of Issue : 2024-11-05
Valid Till : 2027-11-04
Written Confirmation Number : WC-0485
Address of the Firm : Block No. 203, Vaso-Alindra Road, PO Alindra-387510, Tal-Matar Dist. Kheda, Guja...
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PharmaCompass also assists you with knowing the Diflucortolone Valerate API Price utilized in the formulation of products. Diflucortolone Valerate API Price is not always fixed or binding as the Diflucortolone Valerate Price is obtained through a variety of data sources. The Diflucortolone Valerate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neriforte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neriforte, including repackagers and relabelers. The FDA regulates Neriforte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neriforte 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 Neriforte supplier is an individual or a company that provides Neriforte active pharmaceutical ingredient (API) or Neriforte finished formulations upon request. The Neriforte suppliers may include Neriforte API manufacturers, exporters, distributors and traders.
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A Neriforte written confirmation (Neriforte WC) is an official document issued by a regulatory agency to a Neriforte manufacturer, verifying that the manufacturing facility of a Neriforte active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neriforte APIs or Neriforte finished pharmaceutical products to another nation, regulatory agencies frequently require a Neriforte WC (written confirmation) as part of the regulatory process.
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