Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
01 1BIOIBERICA, S. A. U.
02 2API Corporation
03 1CKW Pharma Extract GmbH & Co. K. G.
04 1Celsus Laboratories, Inc.
05 1Changzhou Qianhong Biopharm Co. , Ltd.
06 1Nanjing Jianyou Biochemical Pharmaceutical Co., Ltd.
07 1Nippon Rika Pharmaceuticals Co., Ltd.
08 6OPOCRIN S. p. A.
09 1Qingdao Jiulong Biopharmaceutical Co. , Ltd.
10 1Roman Industries Co., Ltd.
11 1Scientific Protein Laboratories LLC
12 1Smithfield BioScience, Inc.
13 1Syntex S. A.
14 2YANTAI DONGCHENG BIOCHEMICALS CO. , LTD.
15 2Yantai Dongcheng Biochemicals Co. , Ltd.
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
Registration Number : 302MF10020
Registrant's Address : C/Antic Cami de Tordera, 109-119, Palafolls, 08389 Barcelona, Spain
Initial Date of Registration : 2020-01-31
Latest Date of Registration : 2021-10-21
A Heparin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin Sodium, including repackagers and relabelers. The FDA regulates Heparin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin Sodium 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 Heparin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heparin Sodium supplier is an individual or a company that provides Heparin Sodium active pharmaceutical ingredient (API) or Heparin Sodium finished formulations upon request. The Heparin Sodium suppliers may include Heparin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Heparin Sodium 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 Heparin Sodium Drug Master File in Japan (Heparin Sodium JDMF) empowers Heparin Sodium 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 Heparin Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Heparin Sodium 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 Heparin Sodium suppliers with JDMF on PharmaCompass.
We have 13 companies offering Heparin Sodium
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