01 1DSM Nutritional Products Ltd.
02 1Sun Chemical Co., Ltd.
01 1Biotin Biotin
02 1d- biotin
01 1China
02 1Netherlands
Registration Number : 217MF11122
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2006-11-15
Registration Number : 217MF10344
Registrant's Address : 29-3 Shinmachi, Yashio City, Saitama Prefecture
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2006-03-24
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PharmaCompass offers a list of Biotin 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 Biotin manufacturer or Biotin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Biotin manufacturer or Biotin supplier.
PharmaCompass also assists you with knowing the Biotin API Price utilized in the formulation of products. Biotin API Price is not always fixed or binding as the Biotin Price is obtained through a variety of data sources. The Biotin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutavit H2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutavit H2, including repackagers and relabelers. The FDA regulates Lutavit H2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutavit H2 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 Lutavit H2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutavit H2 supplier is an individual or a company that provides Lutavit H2 active pharmaceutical ingredient (API) or Lutavit H2 finished formulations upon request. The Lutavit H2 suppliers may include Lutavit H2 API manufacturers, exporters, distributors and traders.
click here to find a list of Lutavit H2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Lutavit H2 Drug Master File in Japan (Lutavit H2 JDMF) empowers Lutavit H2 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 Lutavit H2 JDMF during the approval evaluation for pharmaceutical products. At the time of Lutavit H2 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 Lutavit H2 suppliers with JDMF on PharmaCompass.
We have 2 companies offering Lutavit H2
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