Marking devices assembler education requirements

1. Semiconductor Devices

The courses in this specialization can also be taken for academic credit as ECEA 5630-5632, part of CU Boulder’s Master of Science in Electrical Engineering degree. Enroll here.\n\nThis Semiconductor Devices specialization is designed to be a deep dive into the fundamentals of the electronic devices that form the backbone of our current integrated circuits technology. You will gain valuable experience in semiconductor physics, pn junctions, metal-semiconductor contacts, bipolar junction...

2. Active Optical Devices

The courses in this specialization can also be taken for academic credit as ECEA 5605-5607, part of CU Boulder’s Master of Science in Electrical Engineering degree. Enroll here.\n\nThis Active Optical Devices specialization is designed to help you gain complete understanding of active optical devices by clearly defining and interconnecting the fundamental physical mechanisms, device design principles, and device performance. You will study and gain active experience with light emitting...

3. Medical Devices Quality Management System - ISO 13485:2016

4.2

(631)

Awareness and Application for the requirements of ISO 13485:2016 for Medical Device Development and QMS...

4. EU Medical Device Regulatory Affairs explained Simply

4.3

(391)

How to get approval to sell Medical Devices within the European Union. Understand regulatory affairs & ISO 13485 2016...

5. Practical Regulatory Affairs 2020 - US FDA Medical Devices

4.4

(726)

A practical course discussing the US FDA Medical Device regulations for real-world situations...

6. ISO 13485 - IQOQPQ - Process Validation for Medical Devices

4.1

(389)

Installation Qualification (IQ), Operational Qualification (OQ) & Performance Qualification (PQ) Medical Devices...

7. Internal audit on Medical Device QMS - ISO 13485:2016

4.3

(578)

Successfully conduct an internal audit based on requirements of ISO 13485:2016 for Medical Device Development and QMS...

8. Medical Device Regulation (MDR): Intro for Device Designers

4.4

(520)

An introduction to the EU's Medical Device Regulation (MDR) for those involved in developing medical devices...

9. ISO 13485 Demystified - Medical Devices' QMS 360° Insights

4

(648)

Deep dive into the world of ISO 13485 international standard for medical devices' QMS, basic concepts & requirements...

10. ISO 13485:2016 - Design and Development of Medical Devices

4.2

(408)

Design and Development of Medical Devices in the perspective of ISO 13485:2016 and Medical Devices Industry...

11. Medical Device Process Validation. ISO 13485. IQ OQ PQ.

4.4

(900)

Validate a process to gain approval to sell medical devices in the EU, U.S. & Internationally. Compliance to ISO 13485...

12. Medical Device Regulation 2017/745 EU regulatory affairs.

4.3

(764)

Understand regulations for medical devices in simple terms to gain market approval of a medical device in the EU...

13. Practical Regulatory Affairs 2020 - European Medical Devices

4.5

(527)

A practical course discussing the EU Medical Device Regulation (MDR) in real-world situations...

14. Electronic & Electrical Devices Maintenance & Troubleshooting

4.3

(515)

This course will give you everything you need to start playing with electronics components and fix electronic devices...

15. A+ 2016: PC Assembly Fundamentals

4.5

(271)

Dive into pc components, assembly, & troubleshooting strategies while preparing for Comp TIA A+ Certification (900 Exam)...

16. Applied ISO14971 Medical Device Risk Management

4.5

(637)

A concise guide to executing ISO 14971 requirements...

17. x86 Assembly Language Programming Masters Course

4.5

(382)

Learn Assembly From A Decade Of Experience...

18. Learn to Design Your Own Boards

4.5

(2,697)

Design a board in 15 hours. Step-by-Step tutorial based on Arduino project (Altium)...

19. ARM Assembly Language From Ground Up™ 1

4.6

(694)

Build over 50 Assembly Programs - ARM Instruction Set, Peripheral Driver Development, Algorithms, DSP routines etc...