Academics and Investigators: Unlocking Clinical Research Potential with the HRB NCTO

Dear Colleagues,

?

Clinical trials and investigations hold immense potential to advance healthcare, improve patient outcomes, and contribute to scientific knowledge. However, navigating the complexities of clinical research can often pose significant challenges. To support you in this critical endeavour, we at the NCTO and our partners in the seven university based Clinical Research Facilities/ Centres (CRF/Cs) who are based at the main teaching hospitals in Ireland offer a comprehensive suite of services designed to facilitate an introduction to and full partnership with the wider clinical research effort within Ireland and into Europe in Medicines, Diagnostics and MedTech.

?

What We Offer

HRB NCTO provides readily accessible guidance, expertise and connectedness to ensure the successful delivery of your clinical study or trial. Our offerings are tailored to support the needs of researchers and research networks at every stage of the clinical research process:

?

Signposting

HRB-NCTO can serve as your primary point of contact, connecting you with Ireland's extensive network of CRF/Cs. Whether you are initiating a new study, looking for national or European partners or seeking to collaborate with industry, our team can help you navigate the landscape of clinical innovation and research.

?

Advisory and Consultancy Services

Our consultancy services offer expert guidance on regulatory pathways and the conduct of clinical research across various fields. We are here to advise you on every aspect of your study, from ethical considerations to compliance with regulatory standards.

?

Study Feasibility

We streamline the process of conducting feasibility assessments, providing oversight through our central feasibility service. Our dedicated resources within CRF/Cs can assist you in navigating local systems and engaging with relevant stakeholders, ensuring your study is well-positioned for success. This service has no charge and feedback is provided within 10 working days.

?

Regulatory, Ethics, and Insurance Support

Navigating the regulatory and ethical requirements for clinical research can be daunting. We offer detailed advice on the necessary documentation and submission processes. Where required, we also facilitate connections with local CRF/Cs for additional support and regulatory bodies, ensuring your study adheres to all relevant guidelines and standards.

?

Quality Assurance

Quality is paramount in clinical research, and we ensure it through our dedicated quality manager who facilitates best practices and harmonisation across the network. Our goal is to guide you how best to maintain the highest standards of quality throughout your study.

Medtech Investigation Guidance Our dedicated Medtech expert provides companies, entrepreneurs and investigators guidance in navigating the clinical research landscape and the many supports available in Ireland. Our Medtech Toolkit offers a concise and clear guide if you are planning a clinical investigation in Ireland.

?

Useful Resources

We offer a wealth of resources, including templates, guidance and signposting to relevant training and education programs. These resources are designed to support you at every stage of your research journey, providing you with the tools you need to succeed. Find them on our website.

?

Let’s Collaborate

Research is vital to the advancement of healthcare, and we are here to support you every step of the way. Whether you are in the early stages of proposal development or are ready to launch your study, the HRB NCTO is ready to assist you.

?

For further information or to discuss how we can support your clinical research endeavours, please do not hesitate to contact us at [email protected]. Together, we can drive innovation and excellence in clinical research across Ireland.

?

Sincerely,

?

Eoghan Cooke

Communications Officer,

HRB - NCTO

?

?