Online Regulatory Affairs Training Courses

We delighted to announce that we have 

partnered with Comply Guru to bring you a library of Online Medical Device Regulatory Affairs Courses.

 

Comply Guru offers industry-leading online and blended training solutions to enable learners to get the knowledge and skills they need, from the same systems and devices they use every day!

Our interactive online courses will span across a range of areas from Medical Device Regulation Basics to the Application of Risk Management & ISO 14971, EU Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) to name a few.
 

We will also be able to cater for any organisations who may be looking for custom training courses in any area of Regulatory Affairs. 

Each one of our courses has been created by our expert team of consultants to ensure that all of our courses deliver you the right knowledge in a meaningful way that will meet your needs.

Take a look at our online course offerings below!

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Online General Overview of EU Medical Device Regulation (MDR) Course

Language: English

Our online interactive course is aimed at anyone working in the

medical device industry sector who is looking for a general

overview of the EU MDR. 

Duration: 2 hours

Release Date: 25th March 2020

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Online EU Medical Device Regulation (MDR) Foundation Course

Language: English

Our online interactive course can take you through the regulation,

not just from an industry perspective, but also from a

Notified Body perspective.

Duration: 16 hours

Release Date: Coming Soon

+ Find Out More

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Online Overview of Risk Management & ISO 14971:2019 [including Key Changes]

Language: English

EN ISO 13485:2016 requires medical device manufactures to implement a

Quality Management System that has a greater emphasis on risk.

This course for medical device manufactures has been developed to meet

this more rigorous focus on risk management.

Duration: 7 hours

Release Date: Coming Soon

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Online Medical Device Single Audit Program (MDSAP) Course

Language: English

Our online interactive course provides an introduction to the Medical Device

Single Audit Program (MDSAP) for Medical Device Clients selling into multiple

jurisdictions and specifically into Canada.

Duration: hours

Release Date: Coming Soon

+ Find Out More

Online In Vitro Diagnostic Medical Devices Regulation (IVDR) Course

Language: English

Our online interactive course provides an introduction to the application

of the key principles and practices required for the new In Vitro Diagnostic

Medical Devices Regulation.

Duration: 7 hours

Release Date: Coming Soon

+ Find Out More

Online Clinical Data for Medical Devices and MEDDEV 2.7/1 Course

Language: English

This online course will offer an interactive overview of Clinical Data Evaluation

for Medical Devices & MEDDEV 2.7/1.

Duration: 7 hours

Release Date: Coming Soon

+ Find Out More

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