Veranova: A CDMO that manages complexity with confidence.
01 1Macfarlan Smith Limited
02 1Pioneer Agro Industries (Pharmaceutical Division) Prop. Sanvin Laboratories Pvt. Ltd.
01 1Buprenorphine Hydrochloride
02 1Buprenorphine hydrochloride
01 1India
02 1U.S.A
Veranova: A CDMO that manages complexity with confidence.
Registration Number : 218MF11027
Registrant's Address : 10 Wheatfield Road, Edinburgh EH11 2QA, United Kingdom
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2013-11-11
Registration Number : 231MF10001
Registrant's Address : 206, Eric House, 16th Road, Chembur, Mumbai-400071. INDIA
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
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PharmaCompass offers a list of Buprenorphine Hydrochloride 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 Buprenorphine Hydrochloride manufacturer or Buprenorphine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Buprenorphine Hydrochloride manufacturer or Buprenorphine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Buprenorphine Hydrochloride API Price utilized in the formulation of products. Buprenorphine Hydrochloride API Price is not always fixed or binding as the Buprenorphine Hydrochloride Price is obtained through a variety of data sources. The Buprenorphine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 6029 M manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6029 M, including repackagers and relabelers. The FDA regulates 6029 M manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6029 M 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 6029 M manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 6029 M supplier is an individual or a company that provides 6029 M active pharmaceutical ingredient (API) or 6029 M finished formulations upon request. The 6029 M suppliers may include 6029 M API manufacturers, exporters, distributors and traders.
click here to find a list of 6029 M 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 6029 M Drug Master File in Japan (6029 M JDMF) empowers 6029 M 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 6029 M JDMF during the approval evaluation for pharmaceutical products. At the time of 6029 M 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 6029 M suppliers with JDMF on PharmaCompass.
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