01 1Procos S. p. A.
01 1Landiolol Hydrochloride
01 1Italy
Registration Number : 304MF10033
Registrant's Address : Via Matteotti 249,28062 CAMERI (NOVARA)/ITALY
Initial Date of Registration : 2022-02-10
Latest Date of Registration : 2022-02-10
A Landiolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Landiolol Hydrochloride, including repackagers and relabelers. The FDA regulates Landiolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Landiolol 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 Landiolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Landiolol Hydrochloride supplier is an individual or a company that provides Landiolol Hydrochloride active pharmaceutical ingredient (API) or Landiolol Hydrochloride finished formulations upon request. The Landiolol Hydrochloride suppliers may include Landiolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Landiolol 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 Landiolol Hydrochloride Drug Master File in Japan (Landiolol Hydrochloride JDMF) empowers Landiolol 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 Landiolol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Landiolol 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 Landiolol Hydrochloride suppliers with JDMF on PharmaCompass.
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