Dr. Michor will attend the annual conference on quality. Please
contact office@michor-consulitng.eu to make an appointment
Webinar: Quality by Design (QbD) and Post-approval change management protocols, 5th June 12
Webinar: eLabeling Medical Devices for the EU Market: Issues and Advantages, 12 June 12
Dr. Michor on the RAPS Board of Directors since Jan 2011
Regulatory consulting services for regulatory strategy, drug development, submissions, pharmacovigilance, LCM and more
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Regulatory consulting services for European CE marking, US FDA 510(k) clearance, Technical files, QM systems, risk management and more
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Interim management, change management, turnaround management, M&As, due diligence and more
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Visit one of our upcoming events or book a convenient in-house training
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