01 1Pharmacia & Upjohn Company LLC
01 1Betamethyl Epoxide
01 1U.S.A
Registration Number : 222MF10213
Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
Initial Date of Registration : 2010-08-05
Latest Date of Registration : 2010-08-05
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PharmaCompass offers a list of Betamethyl Epoxide 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 Betamethyl Epoxide manufacturer or Betamethyl Epoxide supplier for your needs.
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PharmaCompass also assists you with knowing the Betamethyl Epoxide API Price utilized in the formulation of products. Betamethyl Epoxide API Price is not always fixed or binding as the Betamethyl Epoxide Price is obtained through a variety of data sources. The Betamethyl Epoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BETAMETHASONE IMPURITY E [EP IMPURITY] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BETAMETHASONE IMPURITY E [EP IMPURITY], including repackagers and relabelers. The FDA regulates BETAMETHASONE IMPURITY E [EP IMPURITY] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BETAMETHASONE IMPURITY E [EP IMPURITY] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A BETAMETHASONE IMPURITY E [EP IMPURITY] supplier is an individual or a company that provides BETAMETHASONE IMPURITY E [EP IMPURITY] active pharmaceutical ingredient (API) or BETAMETHASONE IMPURITY E [EP IMPURITY] finished formulations upon request. The BETAMETHASONE IMPURITY E [EP IMPURITY] suppliers may include BETAMETHASONE IMPURITY E [EP IMPURITY] API manufacturers, exporters, distributors and traders.
click here to find a list of BETAMETHASONE IMPURITY E [EP IMPURITY] suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The BETAMETHASONE IMPURITY E [EP IMPURITY] Drug Master File in Japan (BETAMETHASONE IMPURITY E [EP IMPURITY] JDMF) empowers BETAMETHASONE IMPURITY E [EP IMPURITY] API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the BETAMETHASONE IMPURITY E [EP IMPURITY] JDMF during the approval evaluation for pharmaceutical products. At the time of BETAMETHASONE IMPURITY E [EP IMPURITY] JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of BETAMETHASONE IMPURITY E [EP IMPURITY] suppliers with JDMF on PharmaCompass.
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