SUSANNE MANZ - Eventura

Death by CAPA - Does your CAPA Program need a CAPA?

2-Day Seminar Completed | Recording and Pre-Registration Available

3-HOUR VIRTUAL SEMINAR ON IQ, OQ, PQ IN THE VERIFICATION AND VALIDATION PROCESS

Duration: 3 Hour

Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)

Duration: 90 Minutes

Effective Internal Audit Program

Duration: 90 Minutes

3-Hour Virtual Seminar on Complaint Handling and Medical Device Reporting and Recalls

Duration: 3 Hour

Big Data – Tools and Trends for Improving your Quality System

Duration: 60 Minutes

Secrets to Writing Effective SOPs for QMS

Duration: 90 Minutes

Top Process Validation Mistakes - And How to Avoid Them

Duration: 90 Minutes

Transforming Your Quality System from Reactive to Proactive

Duration: 90 Minutes

Writing Effective SOPs for Medical Device Quality Management Systems

Duration: 90 Minutes

Production and Process Controls for Medical Devices

Duration: 90 Minutes

Document Controls for Medical Devices

Duration: 90 Minutes

Essentials of Post Market Surveillance that you need to know

Duration: 90 Minutes

Ensuring your Site is Ready for an FDA Inspection

Duration: 90 Minutes

Using Metrics to Monitor and Improve Your Quality System

Duration: 60 Minutes

Audit Like the FDA - Effective Internal Audit Program

2-Day Seminar Completed | Recording and Pre-Registration Available

Medical Device Design Control Essentials Course

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register