01 1Alembic Pharmaceutical limited Unit-III
01 1Aging Life Science Co., Ltd.
01 1trametinib
01 1India
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2025-09-01
Registration Number : 20250901-211-J-1996
Manufacturer Name : Alembic Pharmaceutical limit...
Manufacturer Address : Plot No. 842-843, Village-Karakadi, Taluka–Padra, Vadodara-391 450, Gujarat, INDIA
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PharmaCompass offers a list of Trametinib 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 Trametinib manufacturer or Trametinib supplier for your needs.
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PharmaCompass also assists you with knowing the Trametinib API Price utilized in the formulation of products. Trametinib API Price is not always fixed or binding as the Trametinib Price is obtained through a variety of data sources. The Trametinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trametinib Dimethyl Sulfoxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trametinib Dimethyl Sulfoxide, including repackagers and relabelers. The FDA regulates Trametinib Dimethyl Sulfoxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trametinib Dimethyl Sulfoxide 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 Trametinib Dimethyl Sulfoxide supplier is an individual or a company that provides Trametinib Dimethyl Sulfoxide active pharmaceutical ingredient (API) or Trametinib Dimethyl Sulfoxide finished formulations upon request. The Trametinib Dimethyl Sulfoxide suppliers may include Trametinib Dimethyl Sulfoxide 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 Trametinib Dimethyl Sulfoxide Drug Master File in Korea (Trametinib Dimethyl Sulfoxide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Trametinib Dimethyl Sulfoxide. The MFDS reviews the Trametinib Dimethyl Sulfoxide KDMF as part of the drug registration process and uses the information provided in the Trametinib Dimethyl Sulfoxide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Trametinib Dimethyl Sulfoxide 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 Trametinib Dimethyl Sulfoxide API can apply through the Korea Drug Master File (KDMF).
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