Recorded Webinar Archives - MDPharmaCourses.com

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510(k) Training – Webinar – Traditional 510(k) – FDA Registration – US Medical Device Regulatory + 510(k) Ready Template
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Clean Room Training- Webinar: New ISO 14644:2015, design and construction, proof of continuous compliance, personnel behaviour – RECORDED
Original price was: €275.00.Current price is: €175.00. Add to basket
Clinical Evaluation Course Live Webinar Recorded: Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016
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FDA CAPA Webinar Training – How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation
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GD&T Training – Presentation Webinar – GD&T Geometric Dimensioning and Tolerancing
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ISO 13485:2016 – Design and Development of Medical Devices
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Live Webinar – Technical File Structure according to New Medical Device Regulation – Recorded
Original price was: €265.00.Current price is: €135.00. Add to basket
Medical Device Usability & Human Factor Engineering Webinar Training: Introduction to UX aspects for medical device design
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Medical Devices and applicable Regulations – Commented Interactive Presentation Webinar
Original price was: €195.00.Current price is: €135.00. Add to basket
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New ISO 13485:2016 Medical Device QMS Transition Training – Recorded Webinar
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Recorded Webinar

510(k) Training – Webinar – Traditional 510(k) – FDA Registration – US Medical Device Regulatory + 510(k) Ready Template

Clean Room Training- Webinar: New ISO 14644:2015, design and construction, proof of continuous compliance, personnel behaviour – RECORDED

Clinical Evaluation Course Live Webinar Recorded: Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016

FDA CAPA Webinar Training – How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation

GD&T Training – Presentation Webinar – GD&T Geometric Dimensioning and Tolerancing

ISO 13485:2016 – Design and Development of Medical Devices

Live Webinar – Technical File Structure according to New Medical Device Regulation – Recorded

Medical Device Usability & Human Factor Engineering Webinar Training: Introduction to UX aspects for medical device design

Medical Devices and applicable Regulations – Commented Interactive Presentation Webinar

New ISO 13485:2016 Medical Device QMS Transition Training – Recorded Webinar

Latest Events

Training New MDR Regulation 2017/745 on Medical Devices: technical file structure

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510(k) Training – Webinar – Traditional 510(k) – FDA Registration – US Medical Device Regulatory + 510(k) Ready Template

Clean Room Training- Webinar: New ISO 14644:2015, design and construction, proof of continuous compliance, personnel behaviour – RECORDED

Clinical Evaluation Course Live Webinar Recorded: Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016

FDA CAPA Webinar Training – How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation

GD&T Training – Presentation Webinar – GD&T Geometric Dimensioning and Tolerancing

ISO 13485:2016 – Design and Development of Medical Devices

Live Webinar – Technical File Structure according to New Medical Device Regulation – Recorded

Medical Device Usability & Human Factor Engineering Webinar Training: Introduction to UX aspects for medical device design

Medical Devices and applicable Regulations – Commented Interactive Presentation Webinar

New ISO 13485:2016 Medical Device QMS Transition Training – Recorded Webinar

Latest Events

Training New MDR Regulation 2017/745 on Medical Devices: technical file structure

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Stay Updated!

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