About Briskr academy workshop
An entry level overview to the FDA
This workshop will cover everything from identifying if your product is even considered a device, to understanding requirements, exemptions, costs, and timelines
The attendees will leave with knowledge on:
- The likely classification and regulatory pathway and how to verify this
- Steps to submission and to market, including timeline and general cost ranges
- What to expect in terms of enforcement & inspections from FDA
- And how to manage for compliance
Presenter Michelle Lot: Regulatory Strategist, Principal and Founder of Lean RAQA is a 20-year regulatory and quality professional and earned her Regulatory Affairs Professionals Society certification from Northwestern's Kellogg School of Management. She has corporate experience with manufacturers including Baxter Health Care and served a four-year term on the FDA Device Good Manufacturing Practices Advisory Committee (DGMP).
Since 2010, Michelle’s company, Lean RAQA, has supported 100+ companies with regulatory strategy, regulatory submissions, quality systems compliance, due diligence, technical support services, and grief counseling – because dealing with regulators can be emotionally draining. Her clients delegate all those things to her, so they can focus on winning.
The workshop is free of charge and facilitated in English. Please register upfront!