Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
01 1Phyton Biotech LLC
02 1M/s. Alchem International Private Limited
03 1M/s Emcure Pharmaceuticals Ltd
04 1M/s. Cipla Limited
05 1M/s. Fresenius Kabi Oncology Ltd.,
06 1M/s. Laurus Labs Pvt. Ltd.,
07 1M/s. Mac-Chem Products (India) Pvt. Ltd
08 1MSN Laboratories Pvt. Ltd.
Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
Date of Issue : 2020-04-14
Valid Till : 2022-12-03
Written Confirmation Number : 67771B0D
Address of the Firm : 1527 Cliveden Avenue, Delta, British Columbia. V3M 6P7
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, ...
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A Docetaxel Trihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Docetaxel Trihydrate, including repackagers and relabelers. The FDA regulates Docetaxel Trihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Docetaxel Trihydrate 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 Docetaxel Trihydrate supplier is an individual or a company that provides Docetaxel Trihydrate active pharmaceutical ingredient (API) or Docetaxel Trihydrate finished formulations upon request. The Docetaxel Trihydrate suppliers may include Docetaxel Trihydrate API manufacturers, exporters, distributors and traders.
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A Docetaxel Trihydrate written confirmation (Docetaxel Trihydrate WC) is an official document issued by a regulatory agency to a Docetaxel Trihydrate manufacturer, verifying that the manufacturing facility of a Docetaxel Trihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Docetaxel Trihydrate APIs or Docetaxel Trihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Docetaxel Trihydrate WC (written confirmation) as part of the regulatory process.
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