01 1M/s Sudeep Pharma Pvt ltd
01 1Calcium Carbonate EP/BP/USP
01 1WC-0361
01 1India
Date of Issue : 2022-06-14
Valid Till : 2025-05-20
Written Confirmation Number : WC-0361
Address of the Firm : 129/1/A, GIDC Estate, Nandesari, Vadodara, Gujarat India
65
PharmaCompass offers a list of Calcium Carbonate 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 Calcium Carbonate manufacturer or Calcium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Carbonate manufacturer or Calcium Carbonate supplier.
PharmaCompass also assists you with knowing the Calcium Carbonate API Price utilized in the formulation of products. Calcium Carbonate API Price is not always fixed or binding as the Calcium Carbonate Price is obtained through a variety of data sources. The Calcium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neolite SP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neolite SP, including repackagers and relabelers. The FDA regulates Neolite SP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neolite SP 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 Neolite SP supplier is an individual or a company that provides Neolite SP active pharmaceutical ingredient (API) or Neolite SP finished formulations upon request. The Neolite SP suppliers may include Neolite SP API manufacturers, exporters, distributors and traders.
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A Neolite SP written confirmation (Neolite SP WC) is an official document issued by a regulatory agency to a Neolite SP manufacturer, verifying that the manufacturing facility of a Neolite SP active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neolite SP APIs or Neolite SP finished pharmaceutical products to another nation, regulatory agencies frequently require a Neolite SP WC (written confirmation) as part of the regulatory process.
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