Responsible Conduct of Research (RCR)

This four-part series provides a comprehensive exploration of Good Clinical Practice (GCP), Good Documentation Practice (GDocP), Good Publication Practice (GPP), and Good Writing Practice (GWP). Each session focuses on the principles, ethical standards, and quality requirements that are essential for regulatory compliance and professional excellence in clinical research, scientific documentation, and medical writing. Participants will learn foundational concepts, key guidelines from recognised regulatory and professional organisations, and strategies to enhance compliance, data integrity, and documentation quality. 

Training format

Topic

  • Next: 8 Sep 2025 Live online
  • Also: 2 Feb 2026 Live online

Conducting Clinical Research With Integrity

New for 2025

Live online

This course covers Good Clinical Practice (GCP) principles, ensuring participants understand the ethical and regulatory foundations of clinical research, including integrity, safety, consent, data management, and compliance.

  • 1.5 CPD hours Bite-size
  • Presented by Samaa Al Tabbah
  • Next: 22 Sep 2025 Live online
  • Also: 16 Mar 2026 Live online

Writing Clinical Research with Integrity

New for 2025

Live online

This course covers ethical standards, data integrity, audience tailoring, document structure, clarity, consistency, citation, and tools for quality control and compliance.

  • 1.5 CPD hours Bite-size
  • Presented by Samaa Al Tabbah
  • Next: 29 Sep 2025 Live online
  • Also: 20 Apr 2026 Live online

Publishing Clinical Research with Integrity

New for 2025

Live online

This course will look at ethical research, responsible authorship, and data integrity while addressing conflicts, misconduct, and copyright issues.

  • 1.5 CPD hours Bite-size
  • Presented by Samaa Al Tabbah
  • Next: 15 Sep 2025 Live online
  • Also: 9 Mar 2026 Live online

Documenting Clinical Research with Integrity

Live online

Documentation is crucial for regulatory compliance, ensuring accuracy and integrity in clinical trials and laboratory work. GDP has evolved over time, guided by ALCOA & ALCOA-plus principles.

  • 1.5 CPD hours Bite-size
  • Presented by Samaa Al Tabbah