01 1BASF SE
01 1Parmarine Co., Ltd.
01 1Tocopherol acetate
01 1Germany
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2024-08-09
Registration Number : 20240809-211-J-1635
Manufacturer Name : BASF SE
Manufacturer Address : Carl-Bosch-Strasse 38, 67056 Ludwigshafen, Germany
40
PharmaCompass offers a list of Vitamin E 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 Vitamin E Acetate manufacturer or Vitamin E Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Vitamin E Acetate API Price utilized in the formulation of products. Vitamin E Acetate API Price is not always fixed or binding as the Vitamin E Acetate Price is obtained through a variety of data sources. The Vitamin E Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A INFUVITE ADULT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INFUVITE ADULT, including repackagers and relabelers. The FDA regulates INFUVITE ADULT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INFUVITE ADULT API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A INFUVITE ADULT supplier is an individual or a company that provides INFUVITE ADULT active pharmaceutical ingredient (API) or INFUVITE ADULT finished formulations upon request. The INFUVITE ADULT suppliers may include INFUVITE ADULT API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a INFUVITE ADULT Drug Master File in Korea (INFUVITE ADULT KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of INFUVITE ADULT. The MFDS reviews the INFUVITE ADULT KDMF as part of the drug registration process and uses the information provided in the INFUVITE ADULT KDMF to evaluate the safety and efficacy of the drug.
After submitting a INFUVITE ADULT 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 INFUVITE ADULT API can apply through the Korea Drug Master File (KDMF).
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