Registration Number : 224MF10186
Registrant's Address : 8145 Blazer Drive, Wilmington, DE, 19808, United States
Initial Date of Registration : 2012-09-03
Latest Date of Registration : 2023-07-05
45
PharmaCompass offers a list of Mitotane 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 Mitotane manufacturer or Mitotane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mitotane manufacturer or Mitotane supplier.
PharmaCompass also assists you with knowing the Mitotane API Price utilized in the formulation of products. Mitotane API Price is not always fixed or binding as the Mitotane Price is obtained through a variety of data sources. The Mitotane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ortho,para DDD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ortho,para DDD, including repackagers and relabelers. The FDA regulates ortho,para DDD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ortho,para DDD 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 ortho,para DDD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ortho,para DDD supplier is an individual or a company that provides ortho,para DDD active pharmaceutical ingredient (API) or ortho,para DDD finished formulations upon request. The ortho,para DDD suppliers may include ortho,para DDD API manufacturers, exporters, distributors and traders.
click here to find a list of ortho,para DDD 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 ortho,para DDD Drug Master File in Japan (ortho,para DDD JDMF) empowers ortho,para DDD 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 ortho,para DDD JDMF during the approval evaluation for pharmaceutical products. At the time of ortho,para DDD 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 ortho,para DDD suppliers with JDMF on PharmaCompass.
We have 1 companies offering ortho,para DDD
Get in contact with the supplier of your choice:
