Process Validation (PV) for Medical Device Industry
Gstudy > Courses and seminars > Process Validation (PV) for Medical Device Industry
Engineering & Validation
Quality Assurance
Location: Frontal
Starts at: 09:00
Duration: 3 Days
Language: Hebrew
3-Day Comprehensive Training Program
Master the essential requirements for process validation in medical device manufacturing. This intensive program covers regulatory compliance, statistical analysis, and measurement system validation to ensure robust manufacturing processes.
Duration: 3 Days
Format: Interactive Workshop with Case Studies
CPE Credits: 24 Hours
When: 26.01.26 | 02.02.26 | 09.02.26 9:00-17:00 Gstudy Training center, Haifa, MatamParticipants may register for the full three-day course to gain an in-depth understanding of all related concepts and practices.
Alternatively, each day is structured as an independent seminar with its own learning objectives and practical applications, allowing participants to register for individual days based on their specific interests or professional needs.Who Should Attend
Quality Engineers • Validation Specialists • Regulatory Affairs Professionals • Manufacturing Engineers • Process Development Teams • QA/QC Managers
About Jose (Yossi) Chvaicer, M.Sc.
Mr. Jose Chvaicer graduated in Mechanical Engineering from the State University of Rio de Janeiro, Brazil, and he has a Master’s Degree in Industrial and Management Eng. from the Technion – Israel Institute of Technology, Haifa, Israel. Jose holds a lead auditor certificate from the IIS (ISO9001, ISO13458).He has over 25 years of international experience in the Pharmaceutical Industry. While...
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Registration Information
Early Bird Discount: 30 days in advance
Group Rates: Available for 3+ participants
Corporate Training: Custom programs for 8+ participants
Contact: Gstudy@gsap.co.il