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On July 21st, 2020 at 6PM IL , we are organizing a regulation webinar on “Demystifying Regulatory Pathways” with Michelle Lott- founder and principal of leanRAQA, where she has supported more than 100 companies with regulatory strategy, regulatory submissions, quality systems compliance, due diligence, technical support services and grief counseling. Michelle served a four-year term on the FDA Device Good Manufacturing Practices Advisory Committee (DGMP).
Topics of the webinar will include:
- FDA Risk-Based Medical Device Classification
- Five steps to market
- Challenges ahead
- 10 common pitfalls to avoid
For registration please click here.
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