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PharmaCompass offers a list of Urea API 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 Urea API manufacturer or Urea API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urea API manufacturer or Urea API supplier.
PharmaCompass also assists you with knowing the Urea API API Price utilized in the formulation of products. Urea API API Price is not always fixed or binding as the Urea API Price is obtained through a variety of data sources. The Urea API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-000-872-102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-872-102, including repackagers and relabelers. The FDA regulates MolPort-000-872-102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-872-102 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 MolPort-000-872-102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-000-872-102 supplier is an individual or a company that provides MolPort-000-872-102 active pharmaceutical ingredient (API) or MolPort-000-872-102 finished formulations upon request. The MolPort-000-872-102 suppliers may include MolPort-000-872-102 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-000-872-102 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 MolPort-000-872-102 Drug Master File in Japan (MolPort-000-872-102 JDMF) empowers MolPort-000-872-102 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 MolPort-000-872-102 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-000-872-102 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 MolPort-000-872-102 suppliers with JDMF on PharmaCompass.
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