Our Services
At Tricentric, we work with a range of partners and sectors in order to provide support in the advancement of your research. Our services are responsive, proactive and entirely committed to your aims. We take a comprehensive collaborative approach and our experienced industry specialist consultants work with you to achieve milestones and timelines whilst ensuring compliance.
Our Consultants are highly qualified and have 5 -20 years of industry experience with wide range of therapeutic expertise and local requirements.
PROJECT AND SITE MANAGEMENT SERVICES
We understand that it is vital for you to protect your revenue wherever possible, which is why we work incredibly hard to bring the best possible expertise at a cost-effective rate without ever compromising on attention to detail and providing the support your organisation needs. This begins with our trial site services.
We take the heavy lifting out of ensuring you start your trial in the best possible circumstances. By finding the most promising sites, sourcing patients and capturing key data, we produce better decisions and mitigate any delays by foreseeing challenges ahead.
Our project management, and site management services include:
- Project Management
- Vendor Management
- Study Documents Development
- Site Feasibility - Identification, Qualification and Selection
- Regulatory Consultancy - Competent Authority, Ethics/IRB and Local Submissions and Approvals
- Site Contract and Budget Negotiation, including Payments
- Investigator Meeting (Virtual Inclusive)
- Full Clinical Site Management - Site Initiation, Site Monitoring and Site Close Out
- Project Rescue Services
We can offer support from the beginning to the very end of any project you take on. Because we take pride in our nimble approach and have extensive experience in all aspects of project management, you can depend on our team to navigate any stumbles along the way and keep your project running to the highest possible standards. This includes working to the necessary statutory requirements.
Worldwide REGULATORY Consultancy
Although we’re based in London, we can work with clients all over the world, thanks to our local regulatory experts that can ensure you’re compliant and meeting the standards required for your project.
For UK this includes:
- Medicines and Healthcare products Regulatory Agency (MHRA)
- Research Ethics Committees (REC)/ The Institutional Review Board (IRB) or Independent Ethics Committee (IEC)
- Health Research Authority (HRA)
- National Institute for Health Research (NIHR)
- Central Portfolio Management System (CPMS)
Other Countries Covered:
Austria, Australia, Belgium, Canada, France, Finland, Germany, Ireland, Italy, Netherlands, Norway, Spain, Switzerland, Portugal, USA
Working with us means you can be rest assured that difficult and highly complex administrative work is performed to the highest standards to ensure your project is fully compliant with applicale local requirements.