Join the Twitter conversation about the event - #GCP15
This must-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 (GCP).
About the event
The benefits of attending include:
keeping up to date with GCP requirements and MHRA expectations regarding conduct of clinical trials
learning about the quality issues affecting your organisation
providing an opportunity to share concerns and best practice with others
recognising commonly seen GCP deficiencies and learning how to improving compliance in your organisation
discovering what your peers are doing through managed interactive sessions
meeting the GCP inspectorate team and having the opportunity to ask questions on specific aspects affecting your organisation
Information 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.
Who should attend?
You should attend this event if you are:
those sponsoring and managing clinical trial activities in both the commercial and non-commercial setting
clinical trial pharmacists and technicians
staff collecting, reviewing and reporting clinical trial data such as investigators and research nurses