Rapid execution. Streamlined processes.
inVentiv Health Clinical provides fast recruitment for first-in-man, bioequivalence and proof of concept studies with access to a broad patient population from our extensive, centralized database. The database contains a diverse group of both normal healthy volunteers and special populations patients that can meet a variety of inclusion/exclusion criteria. We also have a favorable mix of new and repeat volunteers.
inVentiv Health Clinical can respond to complex recruitment challenges with novel strategies for a wide range of study criteria.
inVentiv Health Clinical optimizes processes throughout the study to ensure rapid execution. Our project management and regulatory services teams work closely with you to develop a protocol that covers all study parameters while improving study efficiency, data, and timeframes.
We are committed to partnering with our clients, ensuring that all set milestones are met on time. Frequent communication and consultation about the best strategies will provide you with a deep understanding of all options that can lead to a successful study.
inVentiv Health Clinical recognizes the importance of being able to rapidly and accurately handle data. We have invested in an automated process to ensure we can expedite data capture and reporting. Barcodes are used for sample tracking, robust clinical trial management software (CTMS), and electronic data capture (EDC) to reduce potential errors and data verification time while permitting near real-time, transcription-free data access. A best-in-class biostatistics/pharmacometrics team analyzes data using automated and validated systems for rapid compilation of the clinical study report.