CRO Services
Personal and tailored to your requirements.
At BDD, your success is our priority. We provide a comprehensive, full contract research organization (CRO) service with the flexibility to meet your individual program needs. Unlike many UK CROs, our team are co-located within our Phase I Clinical Unit, offering enhanced communication and oversight throughout the project.
From regulatory submissions and expert trial design to full program delivery, we provide a flexible approach that puts you in control. BDD’s CRO services include:
- Clinical Trial Design / Protocol Development
- Regulatory Submissions (MHRA, REC, ARSAC)
- Clinical Project Management
- Site Management
- Pharmacovigilance
- Clinical Trial Monitoring
- Medical monitoring
- TMF Management
- Data Management
- Biostatistics and Statistical Programming
- Medical and Technical Writing
“Cingulate appreciates BDD’s collaborative approach which consistently takes into consideration our priorities. This has allowed us to progress our clinical program for our ADHD clinical candidate. We certainly can recommend BDD for anyone seeking a reliable partner.” – Laurie Myers – Chief Operating Officer
Why Choose BDD?
Streamlined Processes: Our integrated services eliminate the need for separate contracts and coordination between multiple parties making trial initiation and execution more cost effective and efficient.
Communication and Collaboration: We provide a dedicated project manager as a single point of contact who will meet with you weekly throughout the lifecycle of your project. This provides greater clarity and control throughout the trial.
Cross Discipline Expertise: Our unique structure enables us to bring together the combined expertise of our physicians, pharmacists, biopharmaceutical scientists, data experts and GMP specialists to ensure sound, science-based decision making throughout your study.