We Do Think and Do Differently

Providing Seminars in Regulatory Affairs, Quality, Clinical Affairs and Regulatory Compliance to the Global and FDA-Regulated Industry

We help to get empowered by providing practical, actionable and sustainable contents in our seminars.  Please join our seminars and:

  • get well-informed with the latest information for the subject(s);
  • make best decisions – accurate, adequate and effective

Our LIVE online seminars cover, but are not limited to, the following areas:

FDA Compliance 

  • GLP, GCP, and cGMP (QSR)
  • 510(k), PMA, and CE Marking (MDD/AIMDD/IVDD)
  • FDA BIMO inspection
  • MDR
  • Labeling
  • Complaint Handling Systems
  • Unique Device Identification (UDI)
  • FDA Registration and Listing
  • 510(k) and PMA Drafting Seminar Series
  • Many More

Global

  • Global Medical Device Regulations (US, Canada, EU, China, Korea, Japan, Hong Kong, India, Brazil, Mexico, Russia, Latin America, etc.)
  • cGMP: Good Practices
  • CE Mark
  • Technical File and Design Dossier
  • Clinical Evaluation

The contents of our LIVE online seminars (webinars) are adequately designed to help achieve compliance and remain compliant and beyond in our highly regulated healthcare and medical industries.

Last Updated: January 20, 2016

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