01 1Alembic Pharmaceuticals Limited
02 1Dottikon Exclusive Synthesis AG
03 1Hetero Labs Limited Unit-1
04 1Hetero Labs Limited Unit-I
05 1Hetero Labs Limited(Unit-1)
06 1Lonza AG
07 2MSN Laboratories Private Limited
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PharmaCompass offers a list of Osimertinib Mesylate 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 Osimertinib Mesylate manufacturer or Osimertinib Mesylate supplier for your needs.
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PharmaCompass also assists you with knowing the Osimertinib Mesylate API Price utilized in the formulation of products. Osimertinib Mesylate API Price is not always fixed or binding as the Osimertinib Mesylate Price is obtained through a variety of data sources. The Osimertinib Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1421373-66-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1421373-66-1, including repackagers and relabelers. The FDA regulates 1421373-66-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1421373-66-1 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 1421373-66-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1421373-66-1 supplier is an individual or a company that provides 1421373-66-1 active pharmaceutical ingredient (API) or 1421373-66-1 finished formulations upon request. The 1421373-66-1 suppliers may include 1421373-66-1 API manufacturers, exporters, distributors and traders.
click here to find a list of 1421373-66-1 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 1421373-66-1 Drug Master File in Korea (1421373-66-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 1421373-66-1. The MFDS reviews the 1421373-66-1 KDMF as part of the drug registration process and uses the information provided in the 1421373-66-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 1421373-66-1 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 1421373-66-1 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 1421373-66-1 suppliers with KDMF on PharmaCompass.
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