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USDMF
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Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
About the Company : DKSH, founded with the goal of improving people's lives, assists businesses with market expansion and business growth in both existing and emerging markets. It has been fostering g...
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Pharm-Rx has earned an outstanding reputation since its establishment in 1991, serving as a reputable importer and distributor of active ingredients to the pharmaceutical, nutritio...
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
About the Company : Octavius Pharma is a global leader in Directly Compressible Granules with over 40 years of experience in Formulation development, manufacturing and commercialization. It offers a w...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
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62
PharmaCompass offers a list of Aluminium Hydroxide 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 Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier.
PharmaCompass also assists you with knowing the Aluminium Hydroxide API Price utilized in the formulation of products. Aluminium Hydroxide API Price is not always fixed or binding as the Aluminium Hydroxide Price is obtained through a variety of data sources. The Aluminium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALUMINIUM HYDROXIDE DRIED GEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALUMINIUM HYDROXIDE DRIED GEL, including repackagers and relabelers. The FDA regulates ALUMINIUM HYDROXIDE DRIED GEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALUMINIUM HYDROXIDE DRIED GEL 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 ALUMINIUM HYDROXIDE DRIED GEL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALUMINIUM HYDROXIDE DRIED GEL supplier is an individual or a company that provides ALUMINIUM HYDROXIDE DRIED GEL active pharmaceutical ingredient (API) or ALUMINIUM HYDROXIDE DRIED GEL finished formulations upon request. The ALUMINIUM HYDROXIDE DRIED GEL suppliers may include ALUMINIUM HYDROXIDE DRIED GEL API manufacturers, exporters, distributors and traders.
click here to find a list of ALUMINIUM HYDROXIDE DRIED GEL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ALUMINIUM HYDROXIDE DRIED GEL DMF (Drug Master File) is a document detailing the whole manufacturing process of ALUMINIUM HYDROXIDE DRIED GEL active pharmaceutical ingredient (API) in detail. Different forms of ALUMINIUM HYDROXIDE DRIED GEL DMFs exist exist since differing nations have different regulations, such as ALUMINIUM HYDROXIDE DRIED GEL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ALUMINIUM HYDROXIDE DRIED GEL DMF submitted to regulatory agencies in the US is known as a USDMF. ALUMINIUM HYDROXIDE DRIED GEL USDMF includes data on ALUMINIUM HYDROXIDE DRIED GEL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ALUMINIUM HYDROXIDE DRIED GEL USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ALUMINIUM HYDROXIDE DRIED GEL suppliers with USDMF 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 ALUMINIUM HYDROXIDE DRIED GEL Drug Master File in Japan (ALUMINIUM HYDROXIDE DRIED GEL JDMF) empowers ALUMINIUM HYDROXIDE DRIED GEL 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 ALUMINIUM HYDROXIDE DRIED GEL JDMF during the approval evaluation for pharmaceutical products. At the time of ALUMINIUM HYDROXIDE DRIED GEL 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 ALUMINIUM HYDROXIDE DRIED GEL suppliers with JDMF on PharmaCompass.
A ALUMINIUM HYDROXIDE DRIED GEL written confirmation (ALUMINIUM HYDROXIDE DRIED GEL WC) is an official document issued by a regulatory agency to a ALUMINIUM HYDROXIDE DRIED GEL manufacturer, verifying that the manufacturing facility of a ALUMINIUM HYDROXIDE DRIED GEL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ALUMINIUM HYDROXIDE DRIED GEL APIs or ALUMINIUM HYDROXIDE DRIED GEL finished pharmaceutical products to another nation, regulatory agencies frequently require a ALUMINIUM HYDROXIDE DRIED GEL WC (written confirmation) as part of the regulatory process.
click here to find a list of ALUMINIUM HYDROXIDE DRIED GEL suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing ALUMINIUM HYDROXIDE DRIED GEL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ALUMINIUM HYDROXIDE DRIED GEL API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture ALUMINIUM HYDROXIDE DRIED GEL as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain ALUMINIUM HYDROXIDE DRIED GEL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ALUMINIUM HYDROXIDE DRIED GEL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ALUMINIUM HYDROXIDE DRIED GEL suppliers with NDC on PharmaCompass.
ALUMINIUM HYDROXIDE DRIED GEL 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 ALUMINIUM HYDROXIDE DRIED GEL 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 ALUMINIUM HYDROXIDE DRIED GEL GMP manufacturer or ALUMINIUM HYDROXIDE DRIED GEL GMP API supplier for your needs.
A ALUMINIUM HYDROXIDE DRIED GEL CoA (Certificate of Analysis) is a formal document that attests to ALUMINIUM HYDROXIDE DRIED GEL's compliance with ALUMINIUM HYDROXIDE DRIED GEL specifications and serves as a tool for batch-level quality control.
ALUMINIUM HYDROXIDE DRIED GEL CoA mostly includes findings from lab analyses of a specific batch. For each ALUMINIUM HYDROXIDE DRIED GEL 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.
ALUMINIUM HYDROXIDE DRIED GEL may be tested according to a variety of international standards, such as European Pharmacopoeia (ALUMINIUM HYDROXIDE DRIED GEL EP), ALUMINIUM HYDROXIDE DRIED GEL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ALUMINIUM HYDROXIDE DRIED GEL USP).
