Online Training
Literature Search for the Clinical Evaluation
Overview, requirements and structured, stepwise approach for SOTA and S&P
Available Dates & Times
● new dates coming soon
Description
Literature searches are an integral part of the clinical evaluation process. They may be regarded the foundation of the clinical evaluation to define the state-of-the-art therapy on one hand and generate safety and performance endpoints on the other. Clinical evaluation – in turn – is the systematic and planned process to continuously generate, collect, analyze & assess clinical data pertaining to a device in order to demonstrate the safety and performance, including clinical benefits, of the device when used as intended. Clinical evaluation is required under Article 61 and Annex XIV of the European Medical Device Regulation 2017/745 (EU-MDR).
Important aspects of the literature search are: definition of the scope, databases involved, definition of search terms, application of PICO process, definition of inclusion & exclusion criteria and finally the appraisal process. At the end, data-analysis and transfer of the relevant data to the Clinical Evaluation Report (CER). To structure the process, sound literature search protocols are key. The seminar will provide an overview of the requirements to conduct and realize a sound literature search and a systematic, stepwise approach which facilitates the process to obtain compliant literature search reports.
Net price
€ 330.00
- Access to online training
- Presentation slides as handout
- Participation certificates
Overview of covered topics
- Applicable legislation & guidelines
- Sources of literature & requirements
- Content details of the Literature Search Protocol (LSP) & Literature Search Protocol (LSR)
- Interlinks with the Clinical Evaluation
- Suggestions for a systematic & efficient, stepwise approach
- Notified Body Expectations
Purpose of the training
The following targets are aimed at:
- Learning about the requirements and expectation of the legislation
- Providing a sound overview of the literature search process
- Suggesting a systematic, stepwise approach
- Providing a structure for the literature search protocols
- Learning, how a standardized approach will help to conduct the search and appraisal process
Who should attend
- Manufacturer
- Regulatory Affairs Manager
- Clinical Affairs Manager
- Medical Writers
- Personal, directly or indirectly involved in the Clinical Evaluation process
Basic knowledge required
- Basic knowledge in EU-MDR
- Basics in Clinical Evaluation
Presenting experts
Prof. Dr. Markus Balkenhol
Team Leader - Senior Clinical Consultant
AKRA TEAM GmbH
Dr. Anna Spehl
Senior Consultant
AKRA TEAM GmbH
Norchéne BenMadhi
Consultant
AKRA TEAM GmbH
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