01 1DDP Specialty Electronic Materials US 9, LLC
01 1DOW CORNING Q7-9120 Silicone Fluid 350cSt
01 1U.S.A
DOW CORNING Q7-9120 Silicone Fluid 350cSt
Registration Number : 219MF10061
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2007-03-05
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PharmaCompass offers a list of Silicon 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 Silicon manufacturer or Silicon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Silicon manufacturer or Silicon supplier.
PharmaCompass also assists you with knowing the Silicon API Price utilized in the formulation of products. Silicon API Price is not always fixed or binding as the Silicon Price is obtained through a variety of data sources. The Silicon Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A silicio manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of silicio, including repackagers and relabelers. The FDA regulates silicio manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. silicio API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A silicio supplier is an individual or a company that provides silicio active pharmaceutical ingredient (API) or silicio finished formulations upon request. The silicio suppliers may include silicio API manufacturers, exporters, distributors and traders.
click here to find a list of silicio 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 silicio Drug Master File in Japan (silicio JDMF) empowers silicio 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 silicio JDMF during the approval evaluation for pharmaceutical products. At the time of silicio 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 silicio suppliers with JDMF on PharmaCompass.
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