Our Niche Life Sciences Services
Celegence provides the global life sciences industry with consulting services and solutions to support regulatory affairs operations and strategy. We specialize in helping our clients reduce cost and time to market by providing flexible, information-based services. With regulatory expertise that spans all types of products, our global regulatory consultants apply up-to-date robust regulatory intelligence to support product lifecycle management and submission strategies. Our blended onshore & offshore model can be tailored to meet each client’s particular needs. Benefits of our solutions and services include clear visibility and control over diverse product portfolios, increased operational efficiencies, lowered cost and ongoing regulatory compliance.
Our Pharmaceutical Services
Supporting client requirements from creation to maintenance of global and local drug product labeling.
Publishing & ECTD Services
Tackling global submission challenges.
Specialty knowledge across various product types for multiple regulatory documents and application types.
Our Medical Device Services
CER / CEP Writing
CER/CEP writing services to streamline your Clinical Evaluation process.
Post Market Surveillance
Design and implement surveillance processes to increase compliance and reduce risks.
Medical Device Consulting
Addressing a changing regulatory environment.
Our Cross-Industry Services