Speaking Engagements
IMARC staff members often speak at conferences and industry events throughout the year. Here is a listing of upcoming speaking engagements. If you are in the area or attending a conference, please stop by and say hello!
Recent Events
Sandra Maddock of IMARC and Timothy Kulbago of ImageIQ presented a webinar on November 7, 2012.
Imaging in Clinical Trials – Unique Compliance Challenges
Wednesday, November 7, 11:00 am – 12:00 pm EST
When imaging is introduced into a clinical trial, a new layer of complexity is added, and additional considerations with regard to helping sites maintain compliance with the imaging requirements should be implemented. Watch the presentation now »
Sandra Maddock presented an audio conference on September 11, 2012.
Centralized vs Onsite Monitoring – Applying FDA's Risk-based Approach
Tuesday, September 11, 11:30 am - 12:30 pm EST
This audio conference covers:
- An overview of FDA's draft guidance on risk-based monitoring
- Tasks performed during onsite monitoring visits vs. using centralized monitoring
- How centralized and onsite monitoring can be used together
- Challenges of implementing a risk-based monitoring approach
- Identifying the potential risk in conduct of clinical trials
Sandra Maddock and Brandy Smith spoke at a BioEnterprise sponsored event held at Corporate College on September 6, 2012.
Clinical Trials: Differences Between Drugs and Devices
Thursday, September 6, 8:00 am - 12:00 pm
Along with very different regulatory paths to market approval, drugs and medical devices also have different requirements and approaches for clinical studies. This program will compare and contrast the strategy, design and regulation of clinical trials for new drugs versus devices.
Sandra Maddock spoke at OMTEC held June 13-14, 2012.
Running a Clinical Trial: How to Navigate Through the Regulatory Maze
Wednesday, June 13, 1:30 pm - 3:00 pm
Whether you are a company owner, project manager, engineer or assistant, you may be called upon to run a clinical trial or be involved in some way. Attendees will learn about the FAIR Shake™ concept which takes a complicated set of regulations and breaks it into four very simple questions to enable you to make educated decisions as you move through a trial.
The session begins with a "current climate" look at FDA then moves to the "how to" of navigating through regulations, specifically targeting what that will mean to attendees who will return to research settings. This presentation will be highly interactive, using case studies with an orthopaedic focus.
