01 2DDP Specialty Electronic Materials US 9, LLC
01 1LiveoTM Q7-9120 Silicone Fluid, 100 cSt
02 1LiveoTM Q7-9120 Silicone Fluid, 350 cSt
01 2U.S.A
LiveoT.M. Q7-9120 Silicone Fluid, 100 cSt
Registration Number : 303MF10091
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2021-06-07
Latest Date of Registration : 2021-06-07
LiveoT.M. Q7-9120 Silicone Fluid, 350 cSt
Registration Number : 303MF10087
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2021-06-03
Latest Date of Registration : 2021-06-03
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PharmaCompass offers a list of Dimethicone 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 Dimethicone manufacturer or Dimethicone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimethicone manufacturer or Dimethicone supplier.
PharmaCompass also assists you with knowing the Dimethicone API Price utilized in the formulation of products. Dimethicone API Price is not always fixed or binding as the Dimethicone Price is obtained through a variety of data sources. The Dimethicone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FRD 20 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FRD 20, including repackagers and relabelers. The FDA regulates FRD 20 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FRD 20 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 FRD 20 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FRD 20 supplier is an individual or a company that provides FRD 20 active pharmaceutical ingredient (API) or FRD 20 finished formulations upon request. The FRD 20 suppliers may include FRD 20 API manufacturers, exporters, distributors and traders.
click here to find a list of FRD 20 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 FRD 20 Drug Master File in Japan (FRD 20 JDMF) empowers FRD 20 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 FRD 20 JDMF during the approval evaluation for pharmaceutical products. At the time of FRD 20 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 FRD 20 suppliers with JDMF on PharmaCompass.
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