Medical Devices Schedule

A Practical Overview of Pre-Filled Syringes

Medical Technology

11-12

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

Regulatory Affairs

29

20

AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects

Artificial Intelligence (AI) in Life Sciences

11

5

An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices

GxP

14

9

An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals

Regulatory Affairs

8

19

An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices

GxP

21

19

An Introduction to the Design and Development of Medical Devices

Medical Technology

29-30

9-10

An introduction to Risk Management ISO 14971:2019

Regulatory Affairs

27

20

Best Practices for Supplier Qualification in Life Science

GxP

6-7

12-13

Biological Evaluation of Medical Devices

Regulatory Affairs

13-14

Cleanroom Requirements for Medical Device Manufacturers

New for 2026

Regulatory Affairs

23

21

Clinical Evaluation of Medical Device Software and Software as a Medical Device

Clinical Research

28

1

Clinical Research Project Management

Clinical Research

29-1

21-23

Cosmetovigilance

Cosmetics

18-19

8-9

Cyber Security for Medical Devices

Regulatory Affairs

19-20

8-9

Data Integrity and Document Management

GxP

22

8

Dealing With Scientific Journal Reviewers: From Comments to Resubmission

New for 2026

Medical Writing

15

1

FDA Approval Process for Medical Devices

Regulatory Affairs

30-1

1-2

Global Market Access for Medical Device Software

New for 2026

Regulatory Affairs

8-9

30-1

Introduction to the In-Vitro Diagnostic Regulation (IVDR)

Regulatory Affairs

16-17

15-16

Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3

Animal Health

13-14

15-16

Masterclass: Market Authorisation of AI-enabled Medical Devices

Artificial Intelligence (AI) in Life Sciences

29-30

8-9

Medical Device Regulation in the Eurasian Union, Russia and the CIS

Regulatory Affairs

30-1

8-9

Medical Device Regulations in Asia-Pacific Markets

Regulatory Affairs

16-17

Medical Device Regulations in the Middle East and North Africa

Regulatory Affairs

18-19

Medical Device Single Audit Programme (MDSAP)

GxP

25-26

Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

Regulatory Affairs

22-26

Medical Writing for Medical Devices

Medical Writing

25-26

30-1

Metered Dose Inhaler (MDI) Technology

Medical Technology

27-28

7-8

Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products

Updated for 2026

Regulatory Affairs

14-15

Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests

New for 2026

Regulatory Affairs

15

9

Non-Conformance and Corrective Action for Medical Device Manufacturers

Regulatory Affairs

19

10

Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)

New for 2026

Vigilance

10-11

2-3

Process Validation for Medical Devices

GxP

4-5

3-4

Selecting the Best Scientific Journal for Your Research

New for 2026

Medical Writing

13

19

Smart Packaging and Electronic Patient Information

GxP

21

2-3

Sterilization of Medical Devices

GxP

23-24

12-13

Sustainable Product Design for MedTech Engineers and Developers

Medical Technology

7-8

26-27

The 2024 EU AI Act

New for 2026

Artificial Intelligence (AI) in Life Sciences

23

3

The Future of Manufacturing: 3D Printing for Medical Devices

New for 2026

Medical Technology

17

9

The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR

Regulatory Affairs

4

21

UK Conformity Assessed (UKCA) Marking for Medical Devices

Regulatory Affairs

15

21

Understanding Scientific Journal Submission and Publication

New for 2026

Medical Writing

11

16

Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers

Regulatory Affairs

8

30

Medical Devices Training Course Calendar

Our Medical Devices calendar for the next 12 months:

Live online		Feb	Mar	Apr	May	Jun	Jul	Sep	Oct	Nov	Dec	Jan
Live online		2026										2027
A Practical Overview of Pre-Filled Syringes	Medical Technology				11-12					11-12
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK	Regulatory Affairs			29					20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences				11					5
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	GxP				14					9
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals	Regulatory Affairs				8					19
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices	GxP				21					19
An Introduction to the Design and Development of Medical Devices	Medical Technology					29-30					9-10
An introduction to Risk Management ISO 14971:2019	Regulatory Affairs			27					20
Best Practices for Supplier Qualification in Life Science	GxP				6-7					12-13
Biological Evaluation of Medical Devices	Regulatory Affairs						13-14
Cleanroom Requirements for Medical Device Manufacturers New for 2026	Regulatory Affairs	23						21
Clinical Evaluation of Medical Device Software and Software as a Medical Device	Clinical Research			28					1
Clinical Research Project Management	Clinical Research			29-1					21-23
Cosmetovigilance	Cosmetics					18-19					8-9
Cyber Security for Medical Devices	Regulatory Affairs		19-20						8-9
Data Integrity and Document Management	GxP					22					8
Dealing With Scientific Journal Reviewers: From Comments to Resubmission New for 2026	Medical Writing					15					1
FDA Approval Process for Medical Devices	Regulatory Affairs					30-1					1-2
Global Market Access for Medical Device Software New for 2026	Regulatory Affairs					8-9				30-1
Introduction to the In-Vitro Diagnostic Regulation (IVDR)	Regulatory Affairs			16-17					15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3	Animal Health			13-14					15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices	Artificial Intelligence (AI) in Life Sciences					29-30					8-9
Medical Device Regulation in the Eurasian Union, Russia and the CIS	Regulatory Affairs					30-1					8-9
Medical Device Regulations in Asia-Pacific Markets	Regulatory Affairs							16-17
Medical Device Regulations in the Middle East and North Africa	Regulatory Affairs				18-19					18-19
Medical Device Single Audit Programme (MDSAP)	GxP					25-26				25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Regulatory Affairs					22-26
Medical Writing for Medical Devices	Medical Writing					25-26				30-1
Metered Dose Inhaler (MDI) Technology	Medical Technology			27-28					7-8
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Updated for 2026	Regulatory Affairs							14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests New for 2026	Regulatory Affairs				15					9
Non-Conformance and Corrective Action for Medical Device Manufacturers	Regulatory Affairs					19					10
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) New for 2026	Vigilance					10-11					2-3
Process Validation for Medical Devices	GxP					4-5					3-4
Selecting the Best Scientific Journal for Your Research New for 2026	Medical Writing			13					19
Smart Packaging and Electronic Patient Information	GxP				21					2-3
Sterilization of Medical Devices	GxP			23-24					12-13
Sustainable Product Design for MedTech Engineers and Developers	Medical Technology				7-8					26-27
The 2024 EU AI Act New for 2026	Artificial Intelligence (AI) in Life Sciences					23					3
The Future of Manufacturing: 3D Printing for Medical Devices New for 2026	Medical Technology					17					9
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR	Regulatory Affairs		4					21
UK Conformity Assessed (UKCA) Marking for Medical Devices	Regulatory Affairs			15					21
Understanding Scientific Journal Submission and Publication New for 2026	Medical Writing				11					16
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers	Regulatory Affairs					8				30