01 1Ako Kasei Co., Ltd.
02 1Macco Organiques, s. r. o.
03 1Tomita Pharmaceutical Co., Ltd.
01 1Calcium chloride hydrate
02 1Calcium chloride, "Tomita"
03 1Japanese Pharmacopoeia calcium chloride hydrate
01 1Czech Republic
02 2Japan
Japanese Pharmacopoeia Calcium Chloride Hydrate
Registration Number : 229MF10097
Registrant's Address : 329 Sakae, Ako City, Hyogo Prefecture
Initial Date of Registration : 2017-05-16
Latest Date of Registration : 2017-05-16
Registration Number : 223MF10151
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2011-10-14
Latest Date of Registration : 2020-12-18
Registration Number : 217MF10519
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-12-27
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A DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER, including repackagers and relabelers. The FDA regulates DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER 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 DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER supplier is an individual or a company that provides DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER active pharmaceutical ingredient (API) or DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER finished formulations upon request. The DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER suppliers may include DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER API manufacturers, exporters, distributors and traders.
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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 DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER Drug Master File in Japan (DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER JDMF) empowers DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER 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 DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER JDMF during the approval evaluation for pharmaceutical products. At the time of DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER 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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We have 3 companies offering DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER
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