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01 3HyClone Laboratories, INC.
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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
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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
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PharmaCompass offers a list of P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene manufacturer or P-N-Methylaminoazobenzene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred P-N-Methylaminoazobenzene manufacturer or P-N-Methylaminoazobenzene supplier.
PharmaCompass also assists you with knowing the P-N-Methylaminoazobenzene API Price utilized in the formulation of products. P-N-Methylaminoazobenzene API Price is not always fixed or binding as the P-N-Methylaminoazobenzene Price is obtained through a variety of data sources. The P-N-Methylaminoazobenzene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MAB manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MAB, including repackagers and relabelers. The FDA regulates MAB manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MAB 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 MAB supplier is an individual or a company that provides MAB active pharmaceutical ingredient (API) or MAB finished formulations upon request. The MAB suppliers may include MAB API manufacturers, exporters, distributors and traders.
click here to find a list of MAB 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 MAB Drug Master File in Japan (MAB JDMF) empowers MAB 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 MAB JDMF during the approval evaluation for pharmaceutical products. At the time of MAB 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 MAB suppliers with JDMF on PharmaCompass.
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