Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1EUROAPI France
03 1Henan Lihua Pharmaceutical Co., Ltd.
04 1Henan Lihua Pharmaceutical Co.,Ltd.
05 1Symbiotica Specialty Ingredients Sdn. Bhd@Tianjin Tianyao Pharmaceuticals Co., Ltd
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2023-06-22
Registration Number : 20230622-71-B-473-12
Manufacturer Name : Symbiotec Pharmalab Private ...
Manufacturer Address : Plot No: 5, 6, 7 & 8, Special Economic Zone, Phase-II, Pharma zone, Pithampur, Dist. ...
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : AbbVie Korea Inc.
Registration Date : 2019-11-26
Registration Number : 20191126-71-B-422-09
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 La Paterie, VERTOLAYE, 63480 France
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PharmaCompass offers a list of Prednisolone Acetate 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 Prednisolone Acetate manufacturer or Prednisolone Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Prednisolone Acetate API Price utilized in the formulation of products. Prednisolone Acetate API Price is not always fixed or binding as the Prednisolone Acetate Price is obtained through a variety of data sources. The Prednisolone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A METIMYD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METIMYD, including repackagers and relabelers. The FDA regulates METIMYD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METIMYD 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 METIMYD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A METIMYD supplier is an individual or a company that provides METIMYD active pharmaceutical ingredient (API) or METIMYD finished formulations upon request. The METIMYD suppliers may include METIMYD API manufacturers, exporters, distributors and traders.
click here to find a list of METIMYD 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 METIMYD Drug Master File in Korea (METIMYD KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of METIMYD. The MFDS reviews the METIMYD KDMF as part of the drug registration process and uses the information provided in the METIMYD KDMF to evaluate the safety and efficacy of the drug.
After submitting a METIMYD 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 METIMYD API can apply through the Korea Drug Master File (KDMF).
click here to find a list of METIMYD suppliers with KDMF on PharmaCompass.
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