Presented by
Management Forum
Responsible Conduct of Research (RCR): Good Documentation Practice (GDocP) Training Course
Best Practices for Integrity in Clinical Studies
Lunch & Learn
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.
19 May 2025
+ 15 September 2025, 9 February 2026 »
from £175
- Format: Live online
- CPD: 1.5 hours for your records
- Certificate of completion
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Part of Lunch & Learn: Responsible Conduct of Research (RCR) series:
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.
What is Lunch & Learn? Turn your lunch hour into a valuable learning opportunity with our all-new Lunch & Learn category – an exciting twist on the traditional webinar, starting in 2025. These bite-sized, budget-friendly and diverse training sessions are designed to fit seamlessly into your working day, providing a flexible and impactful way to advance your skills without disrupting your busy schedule.
If you’re looking to boost your professional expertise, our Lunch & Learn courses combine the latest insights, expert-led instruction, and practical tools to keep you engaged and evolving — all in the time it takes to enjoy your lunch!
So, what are you waiting for? Learn something new, grow your career, and make every minute count.
From £99! Our Lunch & Learn short courses start from just £99 (early booking price) when you book 5 or more places - any combination of multiple courses for one attendee, or multiple attendees on the same course.
Overview
Good Documentation Practice (GDocP) is essential for regulatory compliance, ensuring accuracy and integrity in clinical trials and laboratory work. Over time, GDocP has evolved, guided by Attributable, Legible, Contemporaneous, Original, and Accurate (ALCOA and ALCOA-plus) principles. Key aspects include maintaining essential records, proper data collection, recording, and ensuring data integrity. Reviewing, reporting, and correcting errors are also crucial for compliance. Effective document control involves handling GMP documents, data backup, retention, and implementing systems to prevent errors. Additionally, auditing and monitoring play a vital role in ensuring quality, with regular monitoring visits, Corrective and Preventive Actions (CAPA), and adverse event reporting helping maintain compliance and data reliability.
This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.
Benefits of attending
- Understand the importance of GDocP in regulatory compliance
- Learn the GDocP essential principles
- Implement accurate, complete, and compliant records in clinical research and laboratory settings
Who should attend?
- Clinical research professionals, including clinical research associates, investigators, and study coordinators
- Medical writers, regulatory writers, and publication professionals
- Quality assurance specialists and compliance officers in pharmaceutical and clinical research organisations
- Anyone involved in clinical trial documentation, regulatory submissions, or scientific publications seeking to improve their understanding of good practices and ethical guidelines
Samaa Al Tabbah
MARS (Medical Agency for Research and Statistics)
Dr. Samaa Al Tabbah holds a B.S. in Medical Laboratory Technology (MLT) from the American University of Beirut (AUB) and a Pharm D. in Clinical Pharmacy from the Lebanese American University (LAU). After graduation, Dr. Al Tabbah held a position as a chief pharmacist at the World Health Organization (WHO), Beirut office. At a later stage, she established a pharmacy in Beirut, where she served as a community pharmacist for over 6 years. Dr. Al Tabbah is a strong supporter of the Children’s Cancer Center in Lebanon where she served as a volunteer for 4 years. She also acts as a consultant and mentor at the Egypt Scholars Inc. and the International Pharmaceutical Students Federation (IPSF) where she works closely with mentees providing them with concrete clinical and research skills that allow them to identify new research topics, discover new techniques, and pursue a strong career development plan.
Through her work, she has been involved in clinical research; more specifically, in training workshops carried out at the national and international level, in the delivery of sessions on different aspects of the conduct of clinical research, as well as in the conduction of different international clinical research projects. She is the author of many scientific papers published in peer-reviewed journals as well as a book titled “The Clinical Research Process from Initiation to Publication”. She is an editorial member of two peer-reviewed scientific journals. She is an Assistant Professor at University Institute for Nursing (Lebanese Red Cross), where she delivers Pharmacology, Microbiology and, Public Health, Community Health, and Clinical Research courses. She was lately appointed as the Global Pharmacovigilance Society Ambassador of Lebanon where she also acts as an acting board member of the society.
19 May 2025
Lunch & Learn
Live online
12:00-13:30 UK (London) (UTC+01)
13:00-14:30 Paris (UTC+02)
07:00-08:30 New York (UTC-04)
Course code 15588
- GBP 175 200
- EUR 245 280
- USD 280 320
Until 12 May
- 90 minutes of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
15 September 2025
Lunch & Learn
Live online
12:00-13:30 UK (London) (UTC+01)
13:00-14:30 Paris (UTC+02)
07:00-08:30 New York (UTC-04)
Course code 15593
- GBP 175 200
- EUR 245 280
- USD 280 320
Until 08 Sep
- 90 minutes of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
9 February 2026
Lunch & Learn
Live online
12:00-13:30 UK (London) (UTC+00)
13:00-14:30 Paris (UTC+01)
07:00-08:30 New York (UTC-05)
Course code 15594
- GBP 175 200
- EUR 245 280
- USD 280 320
Until 02 Feb
- 90 minutes of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
