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