01 1Vifor (International) Inc.
01 1The first iron pellet fumaric acid
01 1Switzerland
Registration Number : 221MF10200
Registrant's Address : Rechenstrasse 37, CH-9001 St. Gallen
Initial Date of Registration : 2009-09-14
Latest Date of Registration : 2016-05-31
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PharmaCompass offers a list of Iron 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 Iron manufacturer or Iron supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iron manufacturer or Iron supplier.
PharmaCompass also assists you with knowing the Iron API Price utilized in the formulation of products. Iron API Price is not always fixed or binding as the Iron Price is obtained through a variety of data sources. The Iron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atomel 95 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atomel 95, including repackagers and relabelers. The FDA regulates Atomel 95 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atomel 95 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 Atomel 95 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atomel 95 supplier is an individual or a company that provides Atomel 95 active pharmaceutical ingredient (API) or Atomel 95 finished formulations upon request. The Atomel 95 suppliers may include Atomel 95 API manufacturers, exporters, distributors and traders.
click here to find a list of Atomel 95 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 Atomel 95 Drug Master File in Japan (Atomel 95 JDMF) empowers Atomel 95 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 Atomel 95 JDMF during the approval evaluation for pharmaceutical products. At the time of Atomel 95 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 Atomel 95 suppliers with JDMF on PharmaCompass.
