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 : 2025-01-28
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PharmaCompass offers a list of Apomorphine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Apomorphine Hydrochloride manufacturer or Apomorphine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Apomorphine Hydrochloride manufacturer or Apomorphine Hydrochloride supplier.
A Apomorphine SL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apomorphine SL, including repackagers and relabelers. The FDA regulates Apomorphine SL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apomorphine SL 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 SL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Apomorphine SL supplier is an individual or a company that provides Apomorphine SL active pharmaceutical ingredient (API) or Apomorphine SL finished formulations upon request. The Apomorphine SL suppliers may include Apomorphine SL API manufacturers, exporters, distributors and traders.
click here to find a list of Apomorphine SL suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 SL Drug Master File in Japan (Apomorphine SL JDMF) empowers Apomorphine SL 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 SL JDMF during the approval evaluation for pharmaceutical products. At the time of Apomorphine SL 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 SL suppliers with JDMF on PharmaCompass.
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