Practical, expert-led GxP training for clinical research professionals. Foundation courses, regulatory updates, and bespoke programmes tailored to your organisation.
Understanding GxP regulations is essential — but applying them effectively in day-to-day clinical research requires more than a one-size-fits-all course. Our training programmes are designed to be relevant, engaging, and directly applicable to the real-world challenges your teams face.
Delivered by an experienced practitioner, all training is available as open courses, bespoke in-house sessions, or virtual webinars — adaptable to your audience and schedule.
To enquire about upcoming courses, request in-house training, or discuss bespoke programme development, please get in touch.
Enquire NowA range of courses covering core GxP disciplines, designed for clinical research professionals at all levels.
A comprehensive introduction to Good Clinical Practice for new entrants and those seeking a solid regulatory grounding. Covers ICH E6(R3), sponsor and investigator obligations, informed consent, and essential documentation.
Stay current with the latest developments in GCP regulation. Covering recent MHRA, EMA, and FDA guidance updates, ICH E6(R3) changes, EU Clinical Trials Regulation, and their practical implications for your clinical programme.
Practical training on building and maintaining effective QMS frameworks in clinical research organisations. Covers SOP development, quality planning, risk management, CAPA, and QMS oversight principles.
Comprehensive training on risk-based monitoring principles as required by ICH E6(R3). Covers risk identification, centralised monitoring, on-site monitoring decisions, and the integration of RBM into the monitoring strategy.
Targeted GCP training for clinical trial site staff — nurses, coordinators, investigators. Practical focus on site responsibilities, delegation, consent, source documentation, and compliance requirements.
We develop and deliver bespoke GxP training programmes tailored to your organisation, SOPs, and specific quality challenges. Ideal for new team onboarding, study start-up, or targeted remediation training.
Open training dates are announced periodically. Contact us to be added to our mailing list for upcoming course notifications.
A full-day open course providing a thorough grounding in GCP for clinical research professionals. Venue and date to be confirmed.
A half-day virtual update covering the latest ICH E6(R3) guidance, EU CTR developments, and MHRA/EMA inspection findings and trends.
To register your interest in any of our courses or to discuss a bespoke training requirement, please get in touch. We will work with you to find the right solution.
We can deliver any course directly at your premises or virtually for your team. All content can be adapted to incorporate your SOPs, systems, and study-specific requirements.
Enquire About In-House Training