Clinical Trial Regulation EU 536/2014 in Clinical Research

Genre: eLearning | Language: English | Duration: 16 Lectures ( 1h 28m ) | Size: 577 MB

A Complete, Certified Course to Implement and Comply with CTR 536/2014 for EU and non-EU Clinical Research Professionals
What you'll learn
Gain an overview of the Clinical Trial Regulation (CTR) to conduct trials in the EU
Understand why changes to the Directive 2001/20/EC were made
Learn and understand the timeline for CTR introduction and transition period
Learn the essential definitions of terms under the CTR
Understand how the Clinical Trial Information System (CTIS) is set up
Understand the submission process of clinical trials
Understand the validation, assessment and decisions process of clinical trials under the CTR
Learn the process to submit a Substantial Modification of the protocol
Learn the process to submit a new Member State in an ongoing study
Identify the safety and other reporting obligations
Grasp the risks and challenges associated with the CTR in sponsor organizations
Practical exercise: Conduct a risk assessment of a regulatory submission with the CTR
Practical exercise: Planning a regulatory submission in line with the CTR
Requirements
No prerequisite is needed for this course.
Description
From 31st January 2023, the Clinical Trial Regulation (CTR) 536/2014 comes into force and repeals the Clinical Trials Directive 2001/20/EC in the European Union (EU). With this Regulation, the EU harmonises the procedures for carrying out clinical trials across the EU states and simplifies the clinical trial approval process through a Clinical Trials Information System (CTIS).This course provide clinical research professionals in Sponsor and CRO organizations as well as investigational sites and study staff with an essential understanding to help implement and comply with the CTR.The programme highlights the most important of these key requirements and how these are impacting all EU as well as non-EU companies conducting clinical trials in the EU.My name is Dr. Vincent Baeyens PhD, I have more than 20 years of experience in running Clinical Trials (phase 1 to 4) in Global and mid-size Pharma, and Biotech settings.Benefits of attending this course include:Gain an overview of the Clinical Trial Regulation (CTR) to conduct trials in the EUUnderstand why changes to the Directive 2001/20/EC were madeLearn and understand the timeline for CTR introduction and transition periodLearn the essential definitions of terms under the CTRUnderstand how the Clinical Trials Information System (CTIS) is set upUnderstand the submission process of clinical trials in the CTISUnderstand the validation, assessment and decisions process of clinical trials under the CTRLearn the process to submit a Substantial Modification of the protocolLearn the process to submit a new Member State in an ongoing studyIdentify the safety and other reporting obligationsGrasp the risks and challenges associated with the CTR in sponsor organizationsPrepare a high-level submission planning under CTRQuizzes and assignments are proposed along your journey to test your knowledge.To facilitate the learning of beginner students, the course has been broken up on purpose in small lectures. If you are a more advanced student, you can increase the speed of lecture to learn the course at your desired pace.Important remark: Please note that this course does not go into the technicalities of the CTIS. References to adequate resources on the topic are provided.Feel free to look at the content of the course to know more and contact me any time if you have any questions!I am looking forward to seeing you inside the course!Sincerely,Vincent
Who this course is for
The course is relevant for all clinical research professionals working in regulatory, clinical operations, project management, pharmacovigilance, quality assurance, vendor/CRO professionals, study sites
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