01 1Piramal Healthcare UK Limited
01 1Misoprostol dispersion
01 1Australia
Registration Number : 303MF10170
Registrant's Address : Whalton Road, Morpeth, Northumberland, NE61 3YA UK
Initial Date of Registration : 2021-12-02
Latest Date of Registration : 2024-08-22
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PharmaCompass offers a list of Misoprostol 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 Misoprostol manufacturer or Misoprostol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Misoprostol manufacturer or Misoprostol supplier.
PharmaCompass also assists you with knowing the Misoprostol API Price utilized in the formulation of products. Misoprostol API Price is not always fixed or binding as the Misoprostol Price is obtained through a variety of data sources. The Misoprostol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ARTHROTEC-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ARTHROTEC-1, including repackagers and relabelers. The FDA regulates ARTHROTEC-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ARTHROTEC-1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ARTHROTEC-1 supplier is an individual or a company that provides ARTHROTEC-1 active pharmaceutical ingredient (API) or ARTHROTEC-1 finished formulations upon request. The ARTHROTEC-1 suppliers may include ARTHROTEC-1 API manufacturers, exporters, distributors and traders.
click here to find a list of ARTHROTEC-1 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 ARTHROTEC-1 Drug Master File in Japan (ARTHROTEC-1 JDMF) empowers ARTHROTEC-1 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 ARTHROTEC-1 JDMF during the approval evaluation for pharmaceutical products. At the time of ARTHROTEC-1 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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