Veranova: A CDMO that manages complexity with confidence.
01 1Macfarlan Smith Limited
01 1Apomorphine hydrochloride
01 1U.S.A
Veranova: A CDMO that manages complexity with confidence.
Registration Number : 223MF10092
Registrant's Address : 10 Wheatfield Road, Edinburgh EH11 2QA, United Kingdom
Initial Date of Registration : 2011-06-29
Latest Date of Registration : 2013-12-10
A Apomorphine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apomorphine Hydrochloride, including repackagers and relabelers. The FDA regulates Apomorphine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apomorphine Hydrochloride 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 Apomorphine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Apomorphine Hydrochloride supplier is an individual or a company that provides Apomorphine Hydrochloride active pharmaceutical ingredient (API) or Apomorphine Hydrochloride finished formulations upon request. The Apomorphine Hydrochloride suppliers may include Apomorphine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Apomorphine Hydrochloride 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 Apomorphine Hydrochloride Drug Master File in Japan (Apomorphine Hydrochloride JDMF) empowers Apomorphine Hydrochloride 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 Apomorphine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Apomorphine Hydrochloride 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 Apomorphine Hydrochloride suppliers with JDMF on PharmaCompass.
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