APRIL 3-5, 2018
Medical Device Quality Congress
Bethesda, MD

MARCH 27, 2018
Improving Your Site Feasibility

• Pre-identify the most likely high-performing sites based on available historical performance data
• Provide advice for tightening up feasibility questionnaires to reduce site burdens
• Give real-world examples of do’s and don’ts in questionnaire development and how to do it more effectively \
• Offer insights into response data review and how to handle discrepancies

APRIL 23, 2018
Managing Cybersecurity Risks in the Medical Device and Healthcare Sectors
Do you know what the FDA, HHS, DHS and global regulators are planning? The cost of ignorance could include regulatory sanctions and liability judgments and cybersecurity attacks are only growing.

APRIL 10-11, 2018
Clinical Quality Assurance: Roles and Responsibilities for Auditors and Managers
Learn what FDA investigators use to evaluate your sites, and how to develop risk-based CQA processes and compliance readiness.
Cambridge, MA