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This program presents advanced concepts by industry experts involved in the research and development of safe and effective medical devices. Add on the Device Basics Preconference Workshop, designed to provide a basic regulatory overview specific to medical device and is a fundamental precursor to the Main Program.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

Presents project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience. 

Information will be presented and discussed regarding the administration of clinical trials according to Health Canada Regulations and International Council for Harmonisation (ICH) guidelines as well as practical procedures and site / sponsor / CRO relationships.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

This conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

This conference, jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

Join us in the Windy City for the SOCRA 2025 Annual Conference hosted at the Hyatt Regency Chicago! 

As the field of research evolves, new ethical and regulatory challenges arise, making it essential for researchers to stay up-to-date with emerging issues. This workshop aims to provide strategies for doing just that.

Unlock the art and science of clinical trial project and program management with this immersive workshop. Whether you're diving into this dynamic field or seeking to enhance your expertise, this program is designed to introduce, affirm, or elevate your understanding of project management in the field of clinical research.

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience. 

This conference, jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

This conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

This interactive workshop is designed to assist Site Coordinators, Research Associates, and Study Nurses in improving their skills and their understanding of the responsibilities of the Clinical Research Site.