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Medical Devices

Duration :

7 hour(s)

Skill level :

Regulatory

Language:

English

Final exam:

Yes

Certificate of Completion:

Yes

CEU / CPD Accreditation:

Yes

Certification:

Gain a recognized and traceable certificate after completing the course :

All our certificates are unique, authentic, CPD/CEU accredited, and FDA 21 CFR PART 11 compliant. Certificates validity can be checked online through our certificate online checker.

Description :

Delve deep into the intricate world of Medical Devices with our tailored learning bundle. Designed for professionals, enthusiasts, and stakeholders, this comprehensive course offers a unique blend of EU and FDA regulations. Whether you’re looking to understand the nuanced differences between EU and FDA Good Manufacturing Practices (GMP) for Medical Devices or aiming to master the latest Medical Device Regulation (MDR 2017/745), this bundle has you covered.

But there’s more. With an exclusive module on Regulatory Compliance Inspections and External Audits, you’ll be equipped with the practical knowledge to navigate inspections with confidence. And with content updated every month, rest assured you’ll always be in tune with the latest in the medical device regulatory landscape.

Join us, and embark on a journey that promises not just learning but a certification of completion, evidencing your newfound expertise. Invest in knowledge that empowers. Secure your place in the evolving world of Medical Devices.

Courses Included :

GMP for Medical Devices and FDA 21 CFR PART 820

1 hour(s)

GMP for Medical Devices: EU versus FDA

2 hour(s)

Medical Device Regulation - MDR 2017/745

2 hour(s)

Regulatory Compliance Inspections and External Audits

2 hour(s)

Your Expert :

Dr. Ciaran McEnister

Senior Pharmaceutical Executive with 25+ years of experience in Medical Device Development, Translational Research, Pharmaceutical development, Pharmacologic/Toxicologic and Preclinical research and Regulatory compliance of small and large molecule drug candidates. Dr. McEnister has an extended experience as senior quality manager.

$320

Participant(s):

Buy now

Large group ? Request a quote !

This course includes:

One-year access

Updated content every month

Certificate of completion

GxP-Training Benefits

Experts : We work with the world's top experts in GMP, GLP, GCP, GDP, regulatory affairs, QA and pharmacovigilance.
Validated : All our courses are CPD/CEU accredited and we deliver a unique, traceable and authentic certificate to each learner.
Self-paced : access 24/7 to the course during 12 months at your own rhythm.
Smooth Experience : Each course starts with a video and ends with an exam and a valid certificate.
Up-to-date : each course is updated on an annual basis to remain valid along the Regulatory Body recommendations.
Instant Purchase : one click to buy and immediate access. Get certified today.
LinkedIn compatible : get a valid certificate at the end of each training program and publish it on LinkedIn with a Unique and Secure Link to your registered certificate.
HR management : all course programs are available either individually or as a batch to HR managers in order to pilot employees Training, follow their progress and send reminders.
Procurement optimized : instant Purchase Order, Online payment and PDF Invoice.
LMS compliant : each course is a SCORM object that you can distribute through your corporate Learning Management System.

Medical Devices

Duration :

7 hour(s)

Skill level :

Regulatory

Language:

English

Final exam:

Yes

Certificate of Completion:

Yes

CEU / CPD Accreditation:

Yes

Certification:

Description :

Courses Included :

Your Expert :

$320

This course includes:

GxP-Training Benefits

Other learning paths

GxP Bundle

Regulatory Affairs Specialist

Validation Engineer

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