CEROVENE’S MANAGEMENT TEAM HAS PROVEN SUCCESS IN DEVELOPING UNIQUE PHARMACEUTICAL PRODUCTS AND GAINING FDA APPROVAL

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OUR TEAM CONSISTS OF INDIVIDUALS HAVING STRONG PHARMACEUTICAL INDUSTRY EXPERIENCE IN THE AREAS OF RESEARCH AND DEVELOPMENT, REGULATORY/QA AND ENGINEERING.  

OUR TEAM HAS A EXCELLENT TRACK RECORD OF DEVELOPING MANUFACTURING, NDA OR ANDA FILING, FDA APPROVAL AND SELLING/LICENSING BOTH GENERIC AND BRANDED PRODUCTS IN THE BOTH U.S AND FOREIGN MARKETS WHILE WORKING FOR SEVERAL PHARMACEUTICAL COMPANIES.

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SCALED-UP LICENSED PRODUCTS AT FIVE MAJOR CMO FACILITIES SUCH AS PATHEON, CATALENT, APTALIS, NORWICH, QS PHARMA, AND AT PARTNER FACILITIES INCLUDING 2 OVERSEAS COMMERCIAL MANUFACTURING SITES.

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54 GENERICS AND 3 NDA'S SUCCESSFULLY DEVELOPED & LICENSED TO 9 DIFFERENT COMPANIES. 

LICENSED GENERIC PRODUCTS CONSIST OF 

MOSTLY EXTENDED-RELEASE PRODUCTS INCLUDING FIRST-TO-FILE

MORE THAN 40% COMMERCIALIZED BY 

PARTNER COMPANY AND 90% ALREADY FILED FOR APPROVAL