01 1Hovione PharmaScience Limited
01 1Doxycycline hyclate
01 1Portugal
Registration Number : 224MF10204
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2012-10-09
Latest Date of Registration : 2024-05-15
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A ACTICLATE CAP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACTICLATE CAP, including repackagers and relabelers. The FDA regulates ACTICLATE CAP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACTICLATE CAP 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 ACTICLATE CAP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ACTICLATE CAP supplier is an individual or a company that provides ACTICLATE CAP active pharmaceutical ingredient (API) or ACTICLATE CAP finished formulations upon request. The ACTICLATE CAP suppliers may include ACTICLATE CAP API manufacturers, exporters, distributors and traders.
click here to find a list of ACTICLATE CAP 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 ACTICLATE CAP Drug Master File in Japan (ACTICLATE CAP JDMF) empowers ACTICLATE CAP 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 ACTICLATE CAP JDMF during the approval evaluation for pharmaceutical products. At the time of ACTICLATE CAP 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 ACTICLATE CAP suppliers with JDMF on PharmaCompass.
