Online Training

UKCA - An Introduction

Understanding the UK Regulatory Landscape and Preparing for Future Regulations

Available Dates & Times

● 16. Oct 2024:   09:00-15:00 h CET
● 13. Nov 2024:   09:00-15:00 h CET
● 13. Dec 2024:   09:00-15:00 h CET

Description

This course is designed to provide a detailed understanding of the UK regulatory landscape for medical devices or in vitro diagnostic devices, focusing on how to navigate current regulations, prepare for future changes, and develop an effective transition strategy.

The training will also cover essential post-market surveillance requirements to ensure ongoing compliance.

This course will help training participants gain in-depth knowledge about the UK’s evolving regulatory environment and learn how to prepare for upcoming changes, including post-market surveillance requirements and developing a robust transition strategy.

Net price

€ 499

Overview of covered topics

Purpose of the training

The following targets are aimed at:

Who should attend

Basic knowledge required

Presenting expert

Hilola Hakimova, MSc

Clinical Consultant
AKRA TEAM GmbH

Dr. Anna Spehl

Senior Consultant
AKRA TEAM GmbH

Norchéne BenMadhi

Consultant
AKRA TEAM GmbH

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