01 1Chongqing Huapont Shengchem Pharmaceutical Co., Ltd.
02 1Olon SPA
03 1Siegfried PharmaChemikalien Minden GmbH
01 1Ace Biopharm Co., Ltd.
02 1CTC Bio Co., Ltd.
03 1DKS Korea Co., Ltd.
01 3Tretinoin
01 1China
02 1Italy
03 1Switzerland
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2021-10-21
Registration Number : 20211021-209-J-1068
Manufacturer Name : Chongqing Huapont Shengchem ...
Manufacturer Address : No. 666 Rongjun Road, Nanjin Avenue Hechuan District, Chongqing China
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2022-12-05
Registration Number : 20221205-209-J-1392
Manufacturer Name : Olon SPA
Manufacturer Address : Via Milano 186 I-20024 Garbagnate Milanese Milano, Italy
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2022-09-26
Registration Number : 20220926-209-J-1368
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstraße 15-39, 42-44 32423 Minden, Germany
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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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AVITA Drug Master File in Korea (AVITA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AVITA. The MFDS reviews the AVITA KDMF as part of the drug registration process and uses the information provided in the AVITA KDMF to evaluate the safety and efficacy of the drug.
After submitting a AVITA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their AVITA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AVITA suppliers with KDMF on PharmaCompass.
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