Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratory Ofichem B. V.
02 1Fuji Chemical Industry Co., Ltd.
03 1Purity Chemicals, S. L.
01 1Zinc Acetate Dihydrate
02 1Zinc acetate 2-hydrate
03 1Zinc acetate hydrate (for manufacturing only)
01 1Japan
02 1Netherlands
03 1Spain
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Registration Number : 304MF10017
Registrant's Address : Heembadweg 5, 9561 CZ Ter apel, The Netherlands
Initial Date of Registration : 2022-01-20
Latest Date of Registration : 2024-02-14
Zinc acetate hydrate (for manufacturing purposes only)
Registration Number : 306MF10011
Registrant's Address : 55 Yokohoonji, Kamiichi-machi, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2024-01-17
Latest Date of Registration : 2024-01-17
Registration Number : 304MF10105
Registrant's Address : Avda. Tren Expresso, Parcelas 82-84 PO Box, 4 34200 Venta de Banos, Palencia, Spain
Initial Date of Registration : 2022-07-27
Latest Date of Registration : 2023-05-10
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PharmaCompass offers a list of Zinc Acetate Dihydrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Zinc Acetate Dihydrate manufacturer or Zinc Acetate Dihydrate supplier for your needs.
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A Acetate Dihydrate, Zinc manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetate Dihydrate, Zinc, including repackagers and relabelers. The FDA regulates Acetate Dihydrate, Zinc manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetate Dihydrate, Zinc API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Acetate Dihydrate, Zinc manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Acetate Dihydrate, Zinc supplier is an individual or a company that provides Acetate Dihydrate, Zinc active pharmaceutical ingredient (API) or Acetate Dihydrate, Zinc finished formulations upon request. The Acetate Dihydrate, Zinc suppliers may include Acetate Dihydrate, Zinc API manufacturers, exporters, distributors and traders.
click here to find a list of Acetate Dihydrate, Zinc suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Acetate Dihydrate, Zinc Drug Master File in Japan (Acetate Dihydrate, Zinc JDMF) empowers Acetate Dihydrate, Zinc API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Acetate Dihydrate, Zinc JDMF during the approval evaluation for pharmaceutical products. At the time of Acetate Dihydrate, Zinc JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Acetate Dihydrate, Zinc suppliers with JDMF on PharmaCompass.
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