Certara is the best-in-class provider of regulatory science, writing, and submission management software and services
Certara is the leading provider of model-informed drug development technology and services, as well as a best-in-class provider of regulatory science, writing, and submission management software and services. Certara’s solutions help inform the drug development and regulatory approval process and address the key efficacy, safety, productivity and commercial challenges facing the biopharma industry. The Company serves 1,200 commercial companies, 250 academic institutions and numerous regulatory agencies, across 60 countries. Certara is headquartered in Princeton, New Jersey with over 850 employees globally, including key operations and senior management in Northern Europe.
Market trends and drivers
Certara operates in fast-growing, niche markets which address critical needs for Certara’s pharma clients. Biosimulation market growth is driven by pharma clients’ need to optimize R&D spend, as well growing regulatory acceptance of model-informed drug development techniques. Regulatory science growth is driven by increasing outsourcing of regulatory writing and the increasing complexity of the regulatory approval process.
EQT VII is keen to support the continued growth of Certara, both domestically and internationally, particularly through continued investment in next generation technology, further international expansion and complementary acquisitions.