Explore
Search CRO profiles and published service listings independently.
Type at least 2 characters to search.
View all results →Our screening and lead identification work starts with the decision your program needs to make. We align on objectives, starting inputs, relevant constraints, and the standard a useful result must meet before we recommend a path forward. By shaping the engagement around those points, we keep technical activity, communication, and deliverables focused on what your team will actually use next.
We approach screening and lead identification by defining success before the first activity starts. We use early scoping to build a sharper request, review the proposed approach, and agree what a decision-ready result will look like. The goal is to find and validate tractable starting points with evidence strong enough to guide investment. Our project plan explains how the work will produce evidence for which hits or candidates should advance, be redesigned, or stop, including what will happen if results fall outside expectations. Early alignment on inputs, assumptions, responsibilities, and review gates is often the difference between useful evidence and an expensive activity report. Give our team enough non-confidential context to challenge assumptions, identify dependencies, and recommend a realistic path. We are a global contract research organization headquartered in Switzerland, providing comprehensive CMC analytical services to pharmaceutical and biotechnology companies. They specialize in analytical development and testing for small molecules, cell and gene therapies, and biologics across all stages of drug development, from early-phase characterization through commercial release testing and stability studies. This context helps establish potential fit. Final selection should depend on project-specific evidence: the proposed scientific lead, relevant examples, methods, capacity, quality status, and timeline. Share the program context, available evidence, constraints, and the decision deadline. Resolve material gaps before the scope and quotation are finalized. Agree the methods, responsibilities, dependencies, controls, acceptance criteria, review points, and change process in one executable plan. Run the work against named milestones. This work sits within our Pre-Clinical Research capabilities and is coordinated with the wider program context when the scope requires it.
Our planning process connects scientific intent with day-to-day execution. We define the question to be answered, map available inputs to the proposed work, identify review gates, and agree on deliverable formats. We also establish how exceptions, missing information, and unexpected findings will be escalated. This gives your team visibility into the work while allowing our specialists to apply sound judgment as the project develops.
Our team treats communication as part of the technical service. We establish contacts, review points, and escalation paths at the outset, then use them to keep decisions moving. Interim conversations distinguish confirmed findings from working interpretations and unresolved questions. That separation is important: it lets the program team act with appropriate confidence while giving specialists space to investigate observations that require more context.
Outputs are planned for the people who will use them next. At kickoff, we agree on the required files, summaries, documentation, and review process rather than assuming a standard package will fit every program. Our final review connects the deliverables back to the original objective and highlights material observations, limitations within the performed scope, and follow-up questions. This makes the handoff more useful for internal review, partner discussions, and subsequent development planning.
A productive first discussion about screening and lead identification usually includes the question to be answered, current program context, available materials or data, target timing, and required outputs. With that foundation, we can identify gaps, explain practical options, and shape a proposal that clearly states activities, inputs, responsibilities, milestones, deliverables, assumptions, and the factors most likely to change scope.
ONE PLATFORM. THREE WAYS TO MOVE FORWARD.
CROaccess helps life science teams move from an open-ended search to a confident partner decision. Choose the level of support that fits your program and your team.
Search CRO profiles and published service listings independently.
Describe your program and receive recommendations aligned with services, stage, and location.
Get hands-on support through outreach, comparison, proposal review, and CRO selection.