Explore how Agos Pharma can streamline your clinical development. Learn more about our approach today.
Clinical Development
At Agos Pharma, we provide a comprehensive suite of clinical development services tailored to meet the unique needs of your product, ensuring that it progresses smoothly from concept through commercialisation.
Our experienced team is dedicated to delivering expert support across each phase of clinical development, with a focus on reducing timelines, ensuring compliance, and maximising your product’s success. Whether you are in early development or preparing for market launch, we are here to support your regulatory, clinical, and operational needs at every stage.
Our Clinical Development Services
We can act as your governance partner in the UK and Europe, overseeing all your CRO activity.
Clinical Research Strategy:
Successful clinical development hinges on a clear, actionable strategy. At Agos Pharma, we work closely with you to craft cost-effective clinical research strategies that align with your product’s goals and market requirements. Our team helps navigate the entire development journey – from pre-clinical phases, through regulatory approvals, to commercial launch. With our expertise, we ensure that critical milestones are met, optimizing your chances of success at every turn.
- Tailored clinical development roadmaps to move your product forward
- Close collaboration to ensure alignment with business and regulatory objectives
- Expert guidance through pre-clinical, clinical, and post-market stages
Feasibility & Site Selection:
A successful study requires the right feasibility studies and site selection. At Agos Pharma, we leverage advanced tools and proven methodologies to conduct thorough feasibility assessments and select optimal sites for recruitment. Our approach goes beyond generic online tools, focusing on data-driven decisions and direct engagement with sites for precise, accurate selection. This helps to optimise study timelines and reduce costs by ensuring that sites are fully equipped to recruit efficiently and meet study demands.
- Thorough feasibility assessments to identify the best study sites
- Engagement with local sites to ensure accurate and actionable data
- Focus on data-driven decisions to avoid common pitfalls
Project Management & Implementation:
Effective project management is essential for ensuring timely study execution. We assign dedicated, experienced Project Managers (PMs) and Clinical Research Associates (CRAs) who maintain continuity throughout the study process. Unlike other CROs, we don’t spread our team across too many projects. By prioritising relationships and stability, we ensure strong recruitment, efficient study implementation, and seamless regulatory compliance.
- Single point of contact for streamlined communication
- Experienced PMs and CRAs to oversee recruitment and study implementation
- Close monitoring to ensure timely execution, adherence to budget, and regulatory requirements
Rescue Studies:
Is your current CRO not delivering on its promises? At Agos Pharma, we specialise in rescuing struggling clinical studies. Whether your CRO is failing to meet deadlines, or issues with project management are threatening the success of your trial, we step in to restore order. Our team can oversee your CRO’s performance, take full ownership of the study, or provide critical support to ensure your trial remains on track and meets all clinical and regulatory objectives.
- Rescue struggling trials with customised intervention plans
- Oversee third-party CROs and restore study integrity
- Maintain regulatory compliance and keep studies aligned with clinical goals
Clinical Trial Submissions
Many smaller pharma and biotech companies have found challenges in the clinical trial approval system in Europe, especially since the introduction of the CTIS. We are experts in gaining approvals. We can help in support from strategic advice to redacting documents.
