01 3HyClone Laboratories, INC.
01 1Medium / medium additive · HyQ ADCF Mab Growth SH3A27 13
02 1Medium / medium additive · HyQ ADCF Mab New Production SH3A2800
03 1Medium / medium additive · HyQ ADCF Mab SH3A2426
01 3U.S.A
Culture medium/culture medium additives HyQ ADCF Mab New Production SH3A2800
Registration Number : 226MF40007
Registrant's Address : 925, West, 1800, South, Logan, Utah, 84321, USA
Initial Date of Registration : 2014-04-15
Latest Date of Registration : 2014-04-15
Culture medium/culture medium additives: HyQ ADCF Mab Growth SH3A2713
Registration Number : 226MF40006
Registrant's Address : 925, West, 1800, South, Logan, Utah, 84321, USA
Initial Date of Registration : 2014-04-15
Latest Date of Registration : 2014-04-15
Culture medium/culture medium additives: HyQ ADCF Mab SH3A2426
Registration Number : 226MF40004
Registrant's Address : 925, West, 1800, South, Logan, Utah, 84321, USA
Initial Date of Registration : 2014-04-15
Latest Date of Registration : 2014-04-15
A P-N-Methylaminoazobenzene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P-N-Methylaminoazobenzene, including repackagers and relabelers. The FDA regulates P-N-Methylaminoazobenzene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene supplier is an individual or a company that provides P-N-Methylaminoazobenzene active pharmaceutical ingredient (API) or P-N-Methylaminoazobenzene finished formulations upon request. The P-N-Methylaminoazobenzene suppliers may include P-N-Methylaminoazobenzene API manufacturers, exporters, distributors and traders.
click here to find a list of P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene Drug Master File in Japan (P-N-Methylaminoazobenzene JDMF) empowers P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene JDMF during the approval evaluation for pharmaceutical products. At the time of P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene suppliers with JDMF on PharmaCompass.
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