The R&D Forum Professional Development – Good Documentation Practice (GDocP) Course
A one-day, in-depth masterclass delivered by trainer Russel Joyce, with advanced clinical records management expertise taking participants through all the key requirements for creating, reviewing, approving, finalising, managing, storing and archiving or preserving essential documents, records, and research data.
Who is the Course for?
This Good Documentation Practice Master Class has been developed to support research management teams to better managing their clinical research documentation and data and is aimed at anyone with responsibility for creating and managing documentation and data within their organisation. As with all R&D Forum activities the course also provides valuable opportunities to meet with colleagues from across the country to discuss challenges and solutions and to share opinions, knowledge, and lived-experiences
Learning Objectives
By the end of this course, participants will be able to:
- Understand the key regulations and legislation that underpin effective document management in clinical research
- Evaluate the strengths and limitations of digital versus hard-copy records
- Confidently manage digital records, including the use of metadata, email, and digital signatures
- Make the most of digital record-keeping tools and technologies
- Apply practical strategies for digital preservation and long-term archiving
- Develop actionable tools and approaches to enhance internal documentation procedures
- Take a risk-based approach to implementing good documentation practice
Prepare more effectively for audits and regulatory inspections
Book your place online:Open Course Details – NHS R&D Forum
