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Data
Management for Medical Device Trials: Best Practices
Helen Colquhoun, MD
CEO Pleiad Devices
Recording
US$199
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recording of this Audio Conference
There
are no regulations in the USA or EU that specifically govern case
report form development or data management practices. There are
some guidelines produced by professional bodies of data managers.
This presentation will cover the range of data management tasks
from CRF design to data entry to raising and resolving queries
to tracking all aspects of data management. There will be a short
discussion of importation of data as well as safety management
as it pertains to data management. Throughout the presentation,
general guidance on best practice will be given.
This
audio conference will cover:
- All the
tasks in a medical device trial that fall under the remit of
data management
- The best
way to complete these tasks
- What systems
and procedures should be in place to ensure compliance with
existing regulatory guidance
- Consequences
of not following best practice
About
the speaker:
Helen
Colquhoun, MD holds degrees in Genetics and Medicine from the
University of Edinburgh and spent several years practising clinical
medicine before entering the life science industry in 1988. Initially
working in the UK in the pharmaceutical industry, Helen set up
as an independent consultant in 1995. Since that time she has
spent increasingly more time working with medical device and drug
delivery companies. In 2000 she co-founded the Pleiad group of
companies and is currently CEO of Pleiad Devices, a clinical research
organization based in the USA and Europe that specializes in clinical
research and regulatory support for medical device companies.
Helen runs Pleiad's North American operation and is based in Cambridge,
Massachusetts.
Who should
attend?
- Data Managers
- Clinical
Project Managers
- Quality
and Regulatory Managers
- Operational
Management Team Members
This
audio conference is classified as General Interest.
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