What you’ll learn
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Become an expert in creating Risk Management documents from scratch, such as PFMEA, DFMEA, FTA, PHA etc for Medical device and Pharmaceutical companies.
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In-depth understanding of Regulatory standards such as ISO 14791:2019, EU 2017/745 MDR, 21 CFR 820, SOR/98-282 and ISO13485.
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Be proficient in what Food and Drug Administration (FDA) auditors are looking for while doing Quality audits for Risk Management activities
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Learn why CAPA, Non conformances, IQ/OQ/PQ, complaint handling process are crucial for medical device industry
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Learn in-depth about Quality Management system (QMS) regulations from different countries around the world
Who this course is for:
- Professionals looking to be promoted or looking to get into medical device or pharmaceutical industry
Can I download Risk Management & QMS for Medical Devices ISO 14971 & 13485. course?
You can download videos for offline viewing in the Android/iOS app. When course instructors enable the downloading feature for lectures of the course, then it can be downloaded for offline viewing on a desktop.Can I get a certificate after completing the course?
Yes, upon successful completion of the course, learners will get the course e-Certification from the course provider. The Risk Management & QMS for Medical Devices ISO 14971 & 13485. course certification is a proof that you completed and passed the course. You can download it, attach it to your resume, share it through social media.Are there any other coupons available for this course?
You can check out for more Udemy coupons @ www.coursecouponclub.com
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Disclosure: This post may contain affiliate links and we may get small commission if you make a purchase. Read more about Affiliate disclosure here.