Registration Number : 222MF10223
Registrant's Address : Great Eastern Chambers, CBD Belapur, Navi Mumbai-400 614, India
Initial Date of Registration : 2010-09-03
Latest Date of Registration : 2013-01-18
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A C040029 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C040029, including repackagers and relabelers. The FDA regulates C040029 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C040029 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 C040029 supplier is an individual or a company that provides C040029 active pharmaceutical ingredient (API) or C040029 finished formulations upon request. The C040029 suppliers may include C040029 API manufacturers, exporters, distributors and traders.
click here to find a list of C040029 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 C040029 Drug Master File in Japan (C040029 JDMF) empowers C040029 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 C040029 JDMF during the approval evaluation for pharmaceutical products. At the time of C040029 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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