Informed Consent

INFORMED CONSENT COURSE INFORMATION

£49

This course is ideal for professionals involved in clinical research, including Clinical Research Associates, Clinical Trial Associates, Clinical Research Coordinators, Principal Investigators, Research Nurses, Clinical Trial Managers, Regulatory Affairs Specialists, Quality Assurance and Compliance Officers, and other study personnel involved in obtaining or supporting the informed consent process.

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£49.00

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KEY FEATURES OF OUR ONLINE INFORMED CONSENT TRAINING COURSE:

100% online and accessible anytime, anywhere
Developed by experts with 35+ years of experience in clinical research
Enhanced with interactive content and robust knowledge checks
Certification on completion

Our Informed Consent training provides a comprehensive overview of one of the most important ethical and regulatory requirements in clinical research. Developed by industry experts with extensive clinical research and quality assurance experience, this course explores the principles of valid informed consent, the consent process, essential documentation, and best practices for ensuring participant understanding, autonomy, and regulatory compliance.

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WHAT WILL I LEARN FROM THIS INFORMED CONSENT TRAINING COURSE?

Understand the definition of informed consent and its importance in protecting the rights, safety, and wellbeing of clinical research participants.

Identify why informed consent is required and the ethical and regulatory principles that underpin the consent process.

Explore the process of obtaining valid informed consent, including documentation, re-consent, withdrawal of consent, and considerations for digital and decentralised studies.

Recognise common challenges that can arise during the informed consent process and apply good practice principles to support compliant, participant-centred consent.

FAQs

Why should I choose this online Informed Consent training course?

Our online Informed Consent course has been developed by experienced clinical research professionals to provide practical, industry-relevant knowledge rather than just theory. Whether you’re new to clinical research or refreshing your knowledge, this course will help you understand the principles of informed consent, meet regulatory expectations, and protect the rights and wellbeing of research participants.

Can I buy this course for my team?

Yes. We offer team licences for organisations of all sizes, making it easy to enrol multiple learners, track their progress and manage training in one place. Please contact us to discuss your requirements and receive a tailored quotation.

Do I need any previous clinical research experience?

No. This course is suitable for learners with little or no previous clinical research experience, as well as professionals looking to refresh or expand their knowledge. The content is presented in a clear, practical way, making it accessible to a wide range of learners.

What makes this course different?

Our training isn’t just a tick-box exercise. Every course is written by experienced clinical research professionals, not AI, and is designed to be engaging, interactive and relevant to real-world practice. Through realistic scenarios, knowledge checks and practical examples, you’ll build confidence in applying what you’ve learned, not just remembering it.