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MHRA GCP symposium 2016

MHRA GCP symposium

Tuesday 20 September 2016

Wednesday 21 September 2016


Join the Twitter conversation about the event at #MHRAGCP

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.

Please only book onto one of the days as the same agenda will run on each day.

We are also hosting MHRA GLP and GCP symposium on the 22nd September 2016.

The event will be held at the Macdonald Burlington Hotel, Birmingham.


Discounts are available to those attending both events.

A limited number of Early-bird rates are available until 5pm, 4th July 2016. Please book early so you don't miss out. Once the allocation of discounted places have been taken, the standard rate will apply.

GCP symposium

  • Early-bird non-commercial rate: 240 + VAT
  • Early-bird industry rate: 450 + VAT
  • Standard non-commercial rate: 295 + VAT
  • Standard industry rate: 575 + VAT

GCP and GLP/GCP Laboratory symposium

  • Early-bird non-commercial rate: 425 + VAT
  • Early-bird industry: 695 + VAT
  • Standard non-commercial rate: 525 + VAT
  • Standard industry rate: 875 + VAT

Benefits of attending:

  • Keep up to date with GCP requirements and MHRA expectations regarding conduct of clinical trials.
  • Recognise the types of compliance issue that organisations have to deal with on a day to day basis and understand how the regulators address these issues on a case by case basis to maintain acceptable levels of compliance and encouraging innovative and flexible thinking.
  • An opportunity to share concerns and best practice with others.
  • Information provided at the event will help you in assessing your own quality systems and potentially identify smart solutions to issues regularly encountered by inspectors and research professionals.
  • 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.
  • Understand how the GCP inspectors address complex compliance issues and learn more about the inspectorates approach to risk based inspection
  • Discuss current hot topics and be aware of areas of compliance that monitoring authorities are likely to focus on during routine inspections.

Register now!

Who should attend?

  • 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
  • Clinical trial co-ordinators and monitors.
  • Anyone planning, conducting, reporting, publishing clinical trials.

Delegates attending the MHRA GCP symposium will be eligible to claim CPD points.

Need more information?

If you have any queries or require further information please e-mail the events team: or telephone on 01772 767726.

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