As the world of clinical research and clinical trials becomes more complex and regulated, budgets are getting tighter and workloads heavier. New European standards and processes, UK governance changes, the emphasis on data privacy and the impact of Covid globally, is creating a heightened sense of awareness within industry that we must move with the times and embrace these challenges.
It is apparent that like it or not, we all need to adapt to change and revise our working practices to ensure delivery and continued quality of new medicines and research. At Centrino we are fully aware of the need to constantly review our processes and ensure compliance and quality standards are always of paramount importance.
Independently we have been working with global pharmaceutical, biotech, and medical device companies since 1991. We have seen many changes during that time and have successfully built upon our experiences to forge strong, robust partnerships, a solid business model and emphasis on dependability.
Our therapeutic experience lies within all study phases of oncology, CNS, respiratory, infectious disease, cardiovascular, vaccines, osteoarthritis, dermatology amongst others. We are driven by our knowledge and experience of managing complex and challenging trials, and we want to share this expertise to help you get your study to the next phase.
Tailor made clinical support services designed around your study
Centrino can assist your clinical study resource requirements, quickly and efficiently. As seasoned clinical program and project managers ourselves, we have a distinct and realistic approach to working with our clients and helping to shape what support is really needed. Unlike many other CROs, we will offer a completely bespoke service, providing support where you need it, and for precisely how long you need it for.
Resourcing engineered around you
If you need help during the last few weeks or months of a clinical study, we can provide project management and coordination to help you get over the final hurdle. We can help with study set-up, initiate sites, advise on TMF and eTMF procedures, write and review SOPs, provide data management support and even data entry. We could provide a handful of days a month or aim to fulfil whatever is required.