Good Clinical Practice
Good Clinical Practice (GCP) is an international ethical and scientific quality standard for the design, conduct, and recording and reporting of research that involve the participation of human subjects. It provides assurance that the rights, safety and well-being of research subjects are protected and that the results of the study are credible. If your research involves human participants you will be asked in your Ethics Application form to give details of Good Clinical Practice (GCP) Training and provide a copy of your training certificate.
Clinical procedures include (but are not limited to):
- Taking human biological samples (blood/ tissue/ saliva etc)
- Use of drugs or medical devices
GCP Training
This core GCP course is for Staff / Research Students who intend to carry out any work at the University of Roehampton in relation to human research procedures. While the principles of GCP that are covered in the course are common to a wide range of different types of research, the workshop tries to instil the ‘GCP-mindset’ needed to satisfy inspectors and auditors. It is therefore mandatory for all Staff/ Research students across the Departments researching in this area. The GCP training course is delivered in collaboration with Research Services.
The next Good Clinical Practice (GCP) training session will be held on Friday, 29 May 2026, from 09:00 to 13:00.
This half-day core course is intended for staff and PhD researchers who plan to undertake work involving human research procedures at the University of Roehampton. While GCP principles apply broadly across many research areas, this session is designed to develop the practical mindset required to meet regulatory, audit, and inspection standards.
Attendance is therefore required for all staff and PhD students engaged in this type of research.
The training will be delivered by Dr Carlucci, an NHS Consultant supporting clinically related research within the Schools of Psychology and Life and Health Sciences at the University of Roehampton.
Venue: G17, Whitelands College, Holybourne Avenue, University of Roehampton, SW15 4JD
Date and time: 29 May 2026, 09:30–13:00
Course outline:
- Core principles of Good Clinical Practice
- Oversight and management of research studies and clinical trials
- Informed consent procedures
- Safety monitoring and adverse event reporting
- Documentation standards, data integrity, and study close-out processes
Learning outcomes:
- By the end of the session, participants will be able to:
- Understand the purpose of GCP, including safeguarding participant rights, confidentiality, and data reliability
- Recognise and apply key GCP principles
- Appreciate the historical context of clinical research and the importance of maintaining high standards
- Understand the current regulatory environment governing clinical research
- Describe the informed consent process and associated responsibilities
- Identify appropriate safety reporting procedures
- Recognise the importance of accurate documentation and data management
- Know where to seek further guidance and support
A CPD training certificate will be issued upon completion of the course.
Please register to secure your place
Please ensure to use your @roehampton email address when booking this training.
If you are unable to attend this course or due to commence your research in the interim before the next scheduled training date, please complete the NHS GCP Training online and retain your Training Certificate - the link to the NHS GCP training is here.
Please note, completion of the online NHS training does not replace completion of the University course and you will still be required to enrol on the annual refresher GCP training.
Good Research Practice and Research Integrity
Good Research Practice underpins high-quality research and includes the principles and responsibilities which ensure that research is planned, conducted, and reported according to the highest achievable standards. Research integrity includes the policies, practices and procedures which ensure those standards are adhered to and which promote a research environment underpinned by a culture of integrity and rigour. The Code of Good Research Practice and Research Integrity sets out the University’s policies, practices and procedures and it is recommended that all research staff familiarise themselves with it.
An online Good Research Practice course also is available via the Medical Research Council at the link here.