Synopsis
0
JDMF
0
KDMF
0
VMF
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Click Us!
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
Axplora- The partner of choice for complex APIs.
EU
Veranova: A CDMO that manages complexity with confidence.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
ASMF
NDC
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
NDC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]INTERMEDIATES SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
Global Sales Information
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Delta-9-Tetrahydrocannabinol And Cannabidiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Delta-9-Tetrahydrocannabinol And Cannabidiol, including repackagers and relabelers. The FDA regulates Delta-9-Tetrahydrocannabinol And Cannabidiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Delta-9-Tetrahydrocannabinol And Cannabidiol supplier is an individual or a company that provides Delta-9-Tetrahydrocannabinol And Cannabidiol active pharmaceutical ingredient (API) or Delta-9-Tetrahydrocannabinol And Cannabidiol finished formulations upon request. The Delta-9-Tetrahydrocannabinol And Cannabidiol suppliers may include Delta-9-Tetrahydrocannabinol And Cannabidiol API manufacturers, exporters, distributors and traders.
click here to find a list of Delta-9-Tetrahydrocannabinol And Cannabidiol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Delta-9-Tetrahydrocannabinol And Cannabidiol DMF (Drug Master File) is a document detailing the whole manufacturing process of Delta-9-Tetrahydrocannabinol And Cannabidiol active pharmaceutical ingredient (API) in detail. Different forms of Delta-9-Tetrahydrocannabinol And Cannabidiol DMFs exist exist since differing nations have different regulations, such as Delta-9-Tetrahydrocannabinol And Cannabidiol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Delta-9-Tetrahydrocannabinol And Cannabidiol DMF submitted to regulatory agencies in the US is known as a USDMF. Delta-9-Tetrahydrocannabinol And Cannabidiol USDMF includes data on Delta-9-Tetrahydrocannabinol And Cannabidiol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Delta-9-Tetrahydrocannabinol And Cannabidiol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Delta-9-Tetrahydrocannabinol And Cannabidiol suppliers with USDMF on PharmaCompass.
A Delta-9-Tetrahydrocannabinol And Cannabidiol CEP of the European Pharmacopoeia monograph is often referred to as a Delta-9-Tetrahydrocannabinol And Cannabidiol Certificate of Suitability (COS). The purpose of a Delta-9-Tetrahydrocannabinol And Cannabidiol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Delta-9-Tetrahydrocannabinol And Cannabidiol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Delta-9-Tetrahydrocannabinol And Cannabidiol to their clients by showing that a Delta-9-Tetrahydrocannabinol And Cannabidiol CEP has been issued for it. The manufacturer submits a Delta-9-Tetrahydrocannabinol And Cannabidiol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Delta-9-Tetrahydrocannabinol And Cannabidiol CEP holder for the record. Additionally, the data presented in the Delta-9-Tetrahydrocannabinol And Cannabidiol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Delta-9-Tetrahydrocannabinol And Cannabidiol DMF.
A Delta-9-Tetrahydrocannabinol And Cannabidiol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Delta-9-Tetrahydrocannabinol And Cannabidiol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Delta-9-Tetrahydrocannabinol And Cannabidiol suppliers with CEP (COS) on PharmaCompass.
A Delta-9-Tetrahydrocannabinol And Cannabidiol written confirmation (Delta-9-Tetrahydrocannabinol And Cannabidiol WC) is an official document issued by a regulatory agency to a Delta-9-Tetrahydrocannabinol And Cannabidiol manufacturer, verifying that the manufacturing facility of a Delta-9-Tetrahydrocannabinol And Cannabidiol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Delta-9-Tetrahydrocannabinol And Cannabidiol APIs or Delta-9-Tetrahydrocannabinol And Cannabidiol finished pharmaceutical products to another nation, regulatory agencies frequently require a Delta-9-Tetrahydrocannabinol And Cannabidiol WC (written confirmation) as part of the regulatory process.
click here to find a list of Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Delta-9-Tetrahydrocannabinol And Cannabidiol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Delta-9-Tetrahydrocannabinol And Cannabidiol suppliers with NDC on PharmaCompass.
Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol 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 Delta-9-Tetrahydrocannabinol And Cannabidiol GMP manufacturer or Delta-9-Tetrahydrocannabinol And Cannabidiol GMP API supplier for your needs.
A Delta-9-Tetrahydrocannabinol And Cannabidiol CoA (Certificate of Analysis) is a formal document that attests to Delta-9-Tetrahydrocannabinol And Cannabidiol's compliance with Delta-9-Tetrahydrocannabinol And Cannabidiol specifications and serves as a tool for batch-level quality control.
Delta-9-Tetrahydrocannabinol And Cannabidiol CoA mostly includes findings from lab analyses of a specific batch. For each Delta-9-Tetrahydrocannabinol And Cannabidiol 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.
Delta-9-Tetrahydrocannabinol And Cannabidiol may be tested according to a variety of international standards, such as European Pharmacopoeia (Delta-9-Tetrahydrocannabinol And Cannabidiol EP), Delta-9-Tetrahydrocannabinol And Cannabidiol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Delta-9-Tetrahydrocannabinol And Cannabidiol USP).
LOOKING FOR A SUPPLIER?
