01 1Kawaken Fine Chemicals Co., Ltd.
02 1Olon S. p. A.
01 1Japanese Pharmacopoeia di Memoru fan phosphate
02 1TRETINOIN type 2
01 1Italy
02 1Japan
Japanese Pharmacopoeia Dimemorfan Phosphate
Registration Number : 219MF10174
Registrant's Address : 2-3-3 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Registration Number : 229MF10001
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2017-01-10
Latest Date of Registration : 2022-12-15
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PharmaCompass offers a list of Tretinoin 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 Tretinoin manufacturer or Tretinoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tretinoin manufacturer or Tretinoin supplier.
PharmaCompass also assists you with knowing the Tretinoin API Price utilized in the formulation of products. Tretinoin API Price is not always fixed or binding as the Tretinoin Price is obtained through a variety of data sources. The Tretinoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AVITA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AVITA, including repackagers and relabelers. The FDA regulates AVITA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AVITA 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 AVITA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AVITA supplier is an individual or a company that provides AVITA active pharmaceutical ingredient (API) or AVITA finished formulations upon request. The AVITA suppliers may include AVITA API manufacturers, exporters, distributors and traders.
click here to find a list of AVITA 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 AVITA Drug Master File in Japan (AVITA JDMF) empowers AVITA 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 AVITA JDMF during the approval evaluation for pharmaceutical products. At the time of AVITA JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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