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Top 3 Most Common Root Cause CAPA Mistakes
⏲ 37 min 12 sec ✓ 04-Aug-2018
Design Controls and Risk Management
⏲ 1 hour 19 minutes 44 seconds 👁 1.1K
The Risk Management of Medical Devices - ISO 14971
⏲ 2 minutes 56 seconds 👁 218
ISO 14971 (Risk Management for Medical Devices) Advanced Course for Lead Auditors | deGRANDSON
⏲ 51 sec ✓ 09-May-2022
ISO 14971 and the risk management of medical devices
⏲ 7 minutes 19 seconds 👁 44
ISO 14971 - 5 Elements of a Risk Management Policy
⏲ 9 minutes 5 seconds 👁 1.9K
Frances Richmond - Risk Assessment and Management Tools - Part 1
⏲ 30 min 27 sec ✓ 28-Aug-2013
What are the four different types of medical device risk analysis?
⏲ 25 minutes 1 second 👁 2.3K
ISO 14971: Using a PHA for Risk Analysis
⏲ 9 minutes 38 seconds 👁 1.7K
Frances Richmond - Risk Assessment and Management Tools - Part 2
⏲ 38 min 21 sec ✓ 28-Aug-2013
Risk Management - Beyond the Basics
⏲ 54 minutes 12 seconds 👁 473
How to work with medical device risk management
⏲ 7 minutes 27 seconds 👁 1.5K
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_top-3-most-common-root-cause-capa-mistakes.webp "Ask yourself one question, and answer it honestly before registering for this webinar: Think of the last 10 corrective actions implemented in your company. On a scale from 1-10, how likely is the same problem to reoccur? How many of them have already reoccurred? nnIf your answer is higher than 2 or 3, then your company, like most companies, is probably bleeding money because of ineffective Root Cause Analysis/Corrective & Preventive Actions. If the corrective actions you are thinking of have")
_design-controls-and-risk-management.webp "leanRAQA")
_the-risk-management-of-medical-devices-iso-14971.webp "Patient Guard Limited")
_iso-14971-risk-management-for-medical-devices-advanced-course-for-lead-auditors-124-degrandson.webp "Online risk management training course for those wishing to manage medical device risk for their companies based on ISO 14971:2019 and ISO/TR 24971:2020. Duration: approximately 16 hours.")
_iso-14971-and-the-risk-management-of-medical-devices.webp "Patient Guard Limited")
_iso-14971-5-elements-of-a-risk-management-policy.webp "Let's Talk Risk!")
_frances-richmond-risk-assessment-and-management-tools-part-1.webp "Frances Richmond, PhDnProfessor and Director, Regulatory Science ProgramnClinical Pharmacy and Pharmaceutical Economics and PolicynnIn this second session, Dr. Frances Richmond introduces us to the concepts of Risk Assessment and Management Tools as formal processes within the Regulatory framework we should all be aware of as clinical translational researchers who work with FDA approved drug or devices. Interestingly, she comments that these important regulatory strategies are “not particularl")
_what-are-the-four-different-types-of-medical-device-risk-analysis.webp "Medical Device Academy")
_iso-14971-using-a-pha-for-risk-analysis.webp "Let's Talk Risk!")
_frances-richmond-risk-assessment-and-management-tools-part-2.webp "Frances Richmond, PhDnProfessor and Director, Regulatory Science ProgramnClinical Pharmacy and Pharmaceutical Economics and PolicynnIn this second session, Dr. Frances Richmond introduces us to the concepts of Risk Assessment and Management Tools as formal processes within the Regulatory framework we should all be aware of as clinical translational researchers who work with FDA approved drug or devices. Interestingly, she comments that these important regulatory strategies are “not particularl")
_risk-management-beyond-the-basics.webp "leanRAQA")
_how-to-work-with-medical-device-risk-management.webp "Medical Device HQ")
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