We rescue poorly performing programs
When poor communication, lack of individual attention, missed deadlines, or subpar deliverables threaten your study’s success, our hands-on leadership, strong governance, and efficient processes restore confidence and put your program back on track.
We know every study is unique, so a one-size-fits-all approach won’t work. Working as a trusted extension of your team, we provide flexible, adaptable support with excellent communication to deliver your projects on time and within budget.
We provide a range of rescue solutions that can be delivered individually or combined to meet your specific needs. As part of our initial review, we conduct a technology assessment to identify potential risks, ensure system compatibility and align with your study requirements.
Data Management
Hands-on, project-based support designed to resolve specific issues and get your study inspection-ready.
Biostatistics
If you’re worried about your study’s design or vendor expertise, our experienced team delivers targeted support and specialist insight, restoring confidence and ensuring reliable results.
Statistical Programming
End-to-end programming expertise to resolve errors, deliver compliant outputs, and restore confidence in your study data.
Strategic Oversight
Embedded senior-level expertise for both operational execution and strategic oversight. Ideal if you want to course-correct CRO performance without fully transitioning Data Management, Biostatistics or Programming
We know that when you need to rescue a study, you need a partner who can quickly take control, rebuild trust, and deliver results.
Better communication and processes: Clear, consistent updates and a structured governance framework keep everyone aligned.
Veramed takes full ownership of deliverables: We act as a true extension of your team, managing every stage of the project with accountability and urgency.
Comprehensive gap analysis: Thorough review of study documentation and processes, including evaluation of existing risks, identification of potential new risks, and detailed analysis of clinical data.
Your study is prioritized: Your timelines and objectives come first, ensuring momentum and focus.
Responsive collaboration: Work side-by-side with a team that’s easy to engage with and aligned to your ways of working.
Customised reporting: Get tailored outputs delivered promptly, aligned to your specifications and decision-making needs.
Smooth transition of vendor, EDC, and lab management: We take control of vendor management and complex handovers, ensuring continuity, quality, and minimal disruption across all partners and systems.
Integrated oversight: Delivered through flexible models, dedicated highly skilled staff, and a fully integrated approach that accelerates timelines, and ensures inspection readiness
Rapid, well-planned transitions that minimise disruption and keep your study moving.
We adjust quickly to evolving study requirements, ensuring momentum is maintained even when priorities shift.
Senior experts guide your rescue project from first conversation to final delivery.
Fast turnaround on agreements, whether using your contracts or ours.
Detailed, honest costings with no hidden fees or unexpected scope changes.
Case studies show our ability to recover struggling projects and deliver on time, every time
Our proven transition methodology ensures a fast, controlled, and quality-focused handover.
Example of our process and timelines:
Initial contact
Discovery (3–5 days)
Definition and planning (7–14 days)
Launch and execution (within 1 month)
