Due to the high demand for an in-depth training on MHRA regulations and after a few successful events attended by over 150 professionals, Astra Nova is organising the next web event that aimes to discuss UK GCP and local requirements and regulations. The Good Clinical Practice – MHRA Regulations webinar serves the purpose to allow professionals access to custom prepared web training, conducted by industry experts with many years of professional experience. The training will discuss some of the most important MHRA GCP topics, such as:
- Understand the MHRA regulatory requirements of Good Clinical Practices (GCP)
- MHRA – Purpose of Monitoring, Auditing & Inspections
- Learn how to set up a clinical study and how to ensure GCP compliance
- Overview of the UK Legislation & Responsibilities in Clinical Trials
The Good Clinical Practice standards ensure the conduct of clinical trials according to the latest regulations and policies. In the UK particularly MHRA is the institution that governs the conduct of clinical trials according to the proper laws and regulations. The international GCP regulations and the MHRA require that all staff is trained to carry out their duties on each study they are working on. Each time when there is an update in the legislation, everyone must get familiar with it and implement it in their working activities.
Astra Nova is a leading training provider for the pharmaceutical, clinical research and biotech industries, organizing custom and off the shelf in-house training solutions, online courses and webinars as well as conferences and seminars. The company does that through the International Network of Trainers, allowing the customers access to over 60 highly experienced industry trainers and professionals. Please visit https://crotraining.co.uk/ to learn more.
