The Art & Science of
Peri- and Post-Approval Clinical Research
Renaissance Associates is a specialized Contract Research Organization (CRO) delivering elite peri- and post-approval trial execution, strategic lifecycle optimization guidance, and scientific data dissemination for the biopharmaceutical and medical device industries.
Expertise Across the Post-Approval Lifecycle
From strategic study planning through execution and scientific dissemination, Renaissance Associates provides specialized expertise to help biopharmaceutical and medical device companies maximize the clinical and commercial value of their products.
Insight
Peri- & Post-Approval Strategic Guidance
Strategic clinical research designed to generate evidence that supports the continued evolution and value of commercialized products.
Evidence
Peri- & Post-Approval Study Conduct
Expert management of post-approval clinical studies from planning through execution. Scientifically rigorous evidence-generation strategies that capitalize on the evolving regulatory environment.
Impact
Data Dissemination Services
Strategies that translate clinical findings into meaningful scientific communications for key audiences.
Engineered for Elite Execution
Senior-Level Expertise
Specialized teams of highly experienced clinical professionals assembled around the needs of each engagement.
Agility & Efficiency
A flexible business model designed to provide senior-level expertise without the overhead and rigidity of a traditional large CRO.
An Extension of Your Team
A highly collaborative approach built on trust, transparency, and seamless integration with internal clinical operations and medical affairs teams.
High-Touch Investigator Relationships
Experienced management of PI and KOL relationships with the professionalism, scientific rigor and regulatory discipline post-approval studies demand.
