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PharmaCompass offers a list of Soberol 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 Soberol manufacturer or Soberol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Soberol manufacturer or Soberol supplier.
PharmaCompass also assists you with knowing the Soberol API Price utilized in the formulation of products. Soberol API Price is not always fixed or binding as the Soberol Price is obtained through a variety of data sources. The Soberol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A sobrerol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sobrerol, including repackagers and relabelers. The FDA regulates sobrerol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sobrerol 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 sobrerol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A sobrerol supplier is an individual or a company that provides sobrerol active pharmaceutical ingredient (API) or sobrerol finished formulations upon request. The sobrerol suppliers may include sobrerol API manufacturers, exporters, distributors and traders.
click here to find a list of sobrerol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A sobrerol DMF (Drug Master File) is a document detailing the whole manufacturing process of sobrerol active pharmaceutical ingredient (API) in detail. Different forms of sobrerol DMFs exist exist since differing nations have different regulations, such as sobrerol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A sobrerol DMF submitted to regulatory agencies in the US is known as a USDMF. sobrerol USDMF includes data on sobrerol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The sobrerol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of sobrerol suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a sobrerol Drug Master File in Korea (sobrerol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of sobrerol. The MFDS reviews the sobrerol KDMF as part of the drug registration process and uses the information provided in the sobrerol KDMF to evaluate the safety and efficacy of the drug.
After submitting a sobrerol KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their sobrerol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of sobrerol suppliers with KDMF on PharmaCompass.
sobrerol Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of sobrerol GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right sobrerol GMP manufacturer or sobrerol GMP API supplier for your needs.
A sobrerol CoA (Certificate of Analysis) is a formal document that attests to sobrerol's compliance with sobrerol specifications and serves as a tool for batch-level quality control.
sobrerol CoA mostly includes findings from lab analyses of a specific batch. For each sobrerol CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
sobrerol may be tested according to a variety of international standards, such as European Pharmacopoeia (sobrerol EP), sobrerol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (sobrerol USP).
