BioXera Pharma: A trusted partner for high-quality human and veterinary APIs and intermediates across global regulated markets.
01 1M/s Bioxera Pharma Pvt Ltd
02 2M/s Benzo Chem Industries Pvt ltd
01 12,4 Dichloro Benzyl Alcohol BP/Ph. Eur
02 12,4-Dichlorobenzyl Alcohol BP/EP
03 12,4-Dichlorobenzyl Alcohol EP
01 1WC-0248
02 1WC-0268
03 1WC-0498
01 3India
BioXera Pharma: A trusted partner for high-quality human and veterinary APIs and intermediates across global regulated markets.
Date of Issue : 2025-12-02
Valid Till : 2028-12-01
Written Confirmation Number : WC-0248
Address of the Firm : Plot No. N-57, Anand Nagar, Additional M.I.D.C., Ambernath (East)-421506, Mahara...
2,4-Dichlorobenzyl Alcohol BP/EP
Date of Issue : 2026-02-13
Valid Till : 2029-01-26
Written Confirmation Number : WC-0268
Address of the Firm : W-24,MIDC,Chemical Zone, Ambernath (West), Ambernath -421501, Dist-Thane, Mahara...
2,4 Dichloro Benzyl Alcohol BP/Ph. Eur
Date of Issue : 2024-09-05
Valid Till : 2027-03-31
Written Confirmation Number : WC-0498
Address of the Firm : E-13/14 & 15, MIDC Area, Ajanta Road, Jalgaon -425003 Taluka: Jalgaon, District ...
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A Tox21_300895 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300895, including repackagers and relabelers. The FDA regulates Tox21_300895 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300895 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 Tox21_300895 supplier is an individual or a company that provides Tox21_300895 active pharmaceutical ingredient (API) or Tox21_300895 finished formulations upon request. The Tox21_300895 suppliers may include Tox21_300895 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300895 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Tox21_300895 written confirmation (Tox21_300895 WC) is an official document issued by a regulatory agency to a Tox21_300895 manufacturer, verifying that the manufacturing facility of a Tox21_300895 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tox21_300895 APIs or Tox21_300895 finished pharmaceutical products to another nation, regulatory agencies frequently require a Tox21_300895 WC (written confirmation) as part of the regulatory process.
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