Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1M/s. Alchem International Private Limited
02 1M/s. Alkaloids Private Limited
01 1Hyoscine (Ph. Eur)
02 1Hyoscine EP
01 1WC-0006
02 1WC-239
01 2India
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Date of Issue : 2022-05-27
Valid Till : 2025-05-26
Written Confirmation Number : WC-0006
Address of the Firm : 25/2, Main Mathura Road, Village Kalli, Ballabgarh, Faridabad-121 004, Haryana, ...
Date of Issue : 2019-11-25
Valid Till : 2022-07-02
Written Confirmation Number : WC-239
Address of the Firm : 25/3, Gundlapochampally, Medchal-Malkajgiri District, Telangana-500 100, India
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PharmaCompass offers a list of Scopolamine 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 Scopolamine manufacturer or Scopolamine supplier for your needs.
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A levo-duboisine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of levo-duboisine, including repackagers and relabelers. The FDA regulates levo-duboisine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. levo-duboisine 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 levo-duboisine supplier is an individual or a company that provides levo-duboisine active pharmaceutical ingredient (API) or levo-duboisine finished formulations upon request. The levo-duboisine suppliers may include levo-duboisine API manufacturers, exporters, distributors and traders.
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A levo-duboisine written confirmation (levo-duboisine WC) is an official document issued by a regulatory agency to a levo-duboisine manufacturer, verifying that the manufacturing facility of a levo-duboisine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting levo-duboisine APIs or levo-duboisine finished pharmaceutical products to another nation, regulatory agencies frequently require a levo-duboisine WC (written confirmation) as part of the regulatory process.
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