the significant demand for our GCP symposium that took place on 3 March 2015, we are pleased to announce that we will be running the symposium
rates are available!
are limited, so book early to avoid disappointment.
non-commercial rate of 240+VAT
industry rate of 495+VAT
Visit www.mhragcp.co.uk to book.
attend annual MHRA event will provide a unique platform for cross-collaboration
and discussion between Regulators and members of the commercial and
non-commercial research community on the latest hot topics and regulatory
updates related to the Good Clinical Practice.
Further information is available on the events website.
Those sponsoring and managing clinical trial activities in
both the commercial and non-commercial setting
trial pharmacists and technicians
collecting, reviewing and reporting clinical trial data such as
investigators and research nurses
Trial co-ordinators and monitors
planning, conducting, reporting, publishing clinical trials.
Benefits of attending:
- Keep up to
date with GCP requirements and MHRA expectations regarding conduct of clinical
- Learn about
the quality issues affecting your organisation.
- An opportunity
to share concerns and best practice with others
provided at the event will help you to move away from burdensome, ineffective
and costly compliance models and provide smart solutions to issues regularly
encountered by inspectors and research professionals.
commonly seen GCP deficiencies and learn how to improve compliance in your
- Discover what
your peers are doing through managed interactive sessions
- Meet the GCP
Inspectorate team and have the opportunity to ask questions on specific aspects
affecting your organisation.
Delegates attending the MHRA GCP
symposium will be eligible to claim CPD points.