Contact us to discuss you team’s training requirements
Training
WFC is a leading provider of training, education, and professional development for the clinical research community, providing confidence from clarity for 15 years. We work across the entire sector, with colleagues from NHS Research & Development (R&D), National Institute for Health and Social Care Research Clinical Research Networks (NIHR CRNs), Clinical Trials Units (CTUs), Higher Education Institutions (HEIs), Medical Research Charities (MRCs) and Industry. All WFC courses and workshops are developed and delivered by trainers with extensive senior experience in their field. We constantly utilise our broad networks to provide the most up-to-date knowledge, ensuring we design all our training to provide clarity for complex issues through interactive, friendly, and engaging sessions. We work with national policy makers so that we know what is forthcoming and can prepare you in advance for what you will be faced with.
We offer a range of bespoke training structures, including half-day workshops and full-day courses. For hosted sessions, WFC trainers will come to the client’s venue and the course is scheduled in accordance with their needs. Virtual training can be delivered remotely to suit a client’s circumstances.
Our approach
We utilise a holistic approach to learning, working with you before, during and after our courses. Uniquely among training providers, WFC provide on-going support and follow-up to delegates, allowing for continued reflection, growth, and development.
Our practical approach to training, education and professional development will help you achieve a competent, confident, and innovative workforce who are motivated to deliver an excellent service. We look forward to working with you to deliver a bespoke solution for your unique requirements.
Our courses - What we do:
Click below to contact us to discuss your training needs. All courses are developed as bespoke.
Recent sessions have focused on the following subjects:
Understanding medical device research - ‘a sponsor’s responsibilities’
Understanding and applying AcoRD principles (including grant costing, the Excess Treatment Cost funding process and using the SoECAT)
Informed consent for research
Monitoring clinical research
Essential documentation management, including Trial Master Files
Protocol development
Regulatory compliance in clinical research