ChemProtel - Product Intelligence is one of the module of Chemxpert, which primarily focus on product related information across all lifesciences industries. ChemProtel covers all products falling under, Pharma API, Pharma Finished Dosages.
ChemProtel covers all products falling under, Pharma API, Pharma Finished Dosages, Pharma Intermediates, Agrochemical Actives, Agro-formulations, Agro-Intermediates, Excipients, Dyes & Pigments, Biologics and Biosimilar, Bio chemicals, Food, Nutraceuticals, Extracts, Polymers, Flavour and fragrances, Veterinary Actives, Veterinary Finished Dosages, Impurities, Antibiotics, Vaccines, Fine and Specialty Chemicals, Enzymes, Basic Chemicals, Inorganic and Organic compounds.
The entire ChemProtel module under Chemxpert database have been classified to facilitates the organized structures of Information as follows:
Basic Information Tab covers, an overview of the molecule such as the Chemical Name, its CAS number, Molecular Weight and Formula, the Innovator and Developer of the molecule, its indication, Therapeutic area and molecule’s approval year.
The Basic information tab can be summarized as below :-
Technical Information Tab provide information regarding the molecules Industry level application, end application, various Route of Synthesis and its Mechanism of Action with access to PDF and excel files available for download.
The Technical Information tab can be summarized as below :-
Commercial Information Tab provides information about the molecules Global Market Size both in Metric Ton as well as Million US Dollars, Average Price in USD per Kg and the US Drug sales.
The Commercial Information tab can be summarized as below :-
Supplier Information Tab provides information related to different suppliers such as their contact details, supplying volume in metric ton, supplier certification and list of countries covered, across the globe.
The Supplier Information tab can be summarized as below :-
Buyers Information Tab this portion buyers such as their contact details, buying volume in metric ton, buyer certification and list of countries covered, across the globe.
The Basic Information tab can be summarized as below :-
Patent Tab includes information regarding the patent expiry, exclusivity and Para IV in the US, SPC and Off-Patent Drugs (No Generics Approved).
The patent tab can be summarized as below :-
Clinical Trial Tab provides information about clinical trials from Phase 0 to IV spanning over various countries for the particular molecule:
Regulatory Fillings / Registration / Approvals Tab provides information about all the INDs, NDAs, establishment license applications, DMFs (Drug Master File), applications for Orphan Drug designation, Fast Track approval application and other similar applications that may be required by any regulatory authority for the development of an API or commercialization of any product.
Regulatory info (Active Pharmaceutical Ingredients) gives information regarding the total number of regulatory filings for a particular drug substance or product.
The Pharma Active Ingredient tab can be summarized as below :-
Regulatory info (Pharma Finished Dosage) refers to finalized product that is meant for sale and consumption.
The Pharma Finished Dosage tab can be summarized as below :-
Certification Tab provides information about the compliance certificates issued for the particular molecule
Warnings & Alerts Tab provides information about number of warning letters or alerts issued for the particular molecule/drug.
All information or part of information can be fetched, by searching the product name or CAS number. The entire information or part of information can be accessed through subscription, for more details, contact us.