Annual Conference

Featuring 100+ speakers presenting in 8 tracks with 21 different sessions/topics and also includes a robust exhibit and poster program.

Clinical Research Professional Certification Preparation and Review Course

This one-day course will aid participants in preparing for the CCRP certification exam through review of FDA and ICH Good Clinical Practice (GCP) guidelines .

New! Harnessing Social Media to Advance Clinical Research

This conference offers clinical research professionals an understanding of the role of social media in the conduct of clinical research, including capabilities, benefits, and ethical and legal considerations.

New! Conducting Clinical Trials in Canada

This conference offers a uniquely Canadian perspective and will assist all clinical research professionals in improving their skills and their understanding of the responsibilities of conducting clinical research in CANADA.

Clinical Science Course

This introductory course features two modules on clinical research regulatory and procedural practices and a medical/ scientific overview .

Clinical Site Coordinator / Manager and GCP Workshop

This workshop, for site coordinators, research associates, and study nurses with 0-5 years experience, will review the responsibilities at the clinical research site.

Monitoring for Clinical Research and GCP Workshop

This interactive workshop, for site monitors, managers or auditors with 0-5 years of experience, will review GCP and clinical research monitoring best practices.

Advanced Site Management: Finance and Productivity Workshop

This workshop, for site managers and research associates, will review billing, budgeting, profitability, and business best practices for clinical research programs.

Project and Program Management for Clinical Research Conference

This conference will review project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference

This two-day 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.

Protecting Human Research Participants: Legal, Ethical, and Practical Considerations

This conference will aid the participant in understanding the legal, ethical and practical considerations related to human subjects research.

Standard Operating Procedures (SOPs) Development and Implementation

This workshop will discuss fundamental concepts in the development and implementation of effective SOPs.

Clinical Trial Management Systems (CTMS) for Clinical Research Programs

This conference will assist the participant in evaluating CTMS capabilities and benefits for their research program and includes exhibits and demonstrations from CTMS vendors.

Device Research Regulations Conference and (optional) Device Basics Preconference

This conference will discuss fundamental concepts and current issues relating to DEVICE research compliance, research development, and clinical investigation for Device Research. An optional half-day program on Device Basics for participants new to device research will precede the main conference.

Clinical Investigator GCP & Trials Management Program

This course, for clinical investigators and key research staff, will review GCP, finance, budgeting and legal responsibilities of the clinical investigative site.

IND/IDE Assistance

This course will discuss issues related to providing IND/IDE assistance, including program start up and successes.

cGMP for Investigational New Drugs (IND) in Phase I Clinical Trials

This course will address the FDA's guidance document regarding cGMP for INDs in Phase I clinical trials

What You Should Know Before the FDA Arrives

This course will discuss the steps involved in an FDA inspection and will address best practice issues in responding to FDA questions.