Unique in Experience & Approach

We strategically design and implement Late Phase Studies for sponsors to optimize clinical and commercial benefits that contribute to a successful product launch and support ongoing commercialization efforts. REGISTRAT personnel collectively apply years of multidisciplinary experience working specifically with the complexities and nuances of Late Phase Studies (peri- and post-approval studies) and observational databases.

Post-marketing Commitments Phase IIIb-IV Studies Disease/Product Registries Pregnancy Registries Risk Management Programs / REMS

Controlled Access Programs / PLAS Safety Surveillance Studies Pharmacoepidemiologic Studies Patient Reported Outcomes Product Commercialization

Complete Spectrum of Late Phase Services

We provide our sponsors a complete spectrum of integrated research services required for conducting Global Late Phase Studies.

Strategic Consulting Clinical Services Safety Management Project Management Data Management Statistical Programming Biostatistics

Quality Assurance Regulatory Management Site Enrollment & Training Call Center EDC & Integrated Technologies Global Reach