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.
Training format
Topic
Lunch & Learn
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.
Lunch & Learn
Live online
This course will look at ethical research, responsible authorship, and data integrity while addressing conflicts, misconduct, and copyright issues.
Lunch & Learn
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.
Lunch & Learn
Live online
This course covers ethical standards, data integrity, audience tailoring, document structure, clarity, consistency, citation, and tools for quality control and compliance.
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