TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI Czech Industries s. r. o.
02 1CONCORD BIOTECH LIMITED.
01 1Mycophenolate mofetil "Teva"
02 1Mycophenolate mofetil (production only)
01 1India
02 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 224MF10107
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2012-06-22
Latest Date of Registration : 2013-05-22
Mycophenolate mofetil (for manufacturing only)
Registration Number : 224MF10054
Registrant's Address : 1482-1486, Trasad Road, Dholka, Dist. Ahmedabad-382225, Gujarat, INDIA
Initial Date of Registration : 2012-03-12
Latest Date of Registration : 2018-12-11
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PharmaCompass offers a list of Mycophenolate Mofetil 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 Mycophenolate Mofetil manufacturer or Mycophenolate Mofetil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mycophenolate Mofetil manufacturer or Mycophenolate Mofetil supplier.
PharmaCompass also assists you with knowing the Mycophenolate Mofetil API Price utilized in the formulation of products. Mycophenolate Mofetil API Price is not always fixed or binding as the Mycophenolate Mofetil Price is obtained through a variety of data sources. The Mycophenolate Mofetil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CellCept Oral Suspension manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CellCept Oral Suspension, including repackagers and relabelers. The FDA regulates CellCept Oral Suspension manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CellCept Oral Suspension 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 CellCept Oral Suspension manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CellCept Oral Suspension supplier is an individual or a company that provides CellCept Oral Suspension active pharmaceutical ingredient (API) or CellCept Oral Suspension finished formulations upon request. The CellCept Oral Suspension suppliers may include CellCept Oral Suspension API manufacturers, exporters, distributors and traders.
click here to find a list of CellCept Oral Suspension 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 CellCept Oral Suspension Drug Master File in Japan (CellCept Oral Suspension JDMF) empowers CellCept Oral Suspension 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 CellCept Oral Suspension JDMF during the approval evaluation for pharmaceutical products. At the time of CellCept Oral Suspension 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 CellCept Oral Suspension suppliers with JDMF on PharmaCompass.
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