In this Training Bulletin we share with you upcoming events as part of the ACDM Training Programme.
Regulatory Guidelines Refresh for Data Managers
Did you know that regulatory inspectors will be looking for evidence that you have received updated GCP & Regulations training every 2 years? This webinar will provide you with an insight into how current regulations and guidelines need to be applied in the data management arena in order to ensure effective compliance with relevant laws. The training course is updated annually so that you can be sure you have the most up to date information. This webinar is for anyone working in data management on clinical trials. Why not gather a group together to ensure your team is up to date.
This webinar is aimed at Data Managers, Project Managers, Clinical Research Associates, Drug Safety specialists and Quality Assurance personnel.
Date: 15th June 2018
Further details: https://www.acdmglobal.org/training-courses/entry/12/
Level Two Accredited Training Program in Clinical Data Management – Technical Skills
Regulators are increasingly requesting evidence of competence. Experience alone does not provide evidence of competence. The ACDM, in partnership with the International Academy of Clinical Research, has developed a series of training programs supported by comprehensive course work and interactive sessions, providing independently recognized, competence-based accreditation to support the continued professional development of staff involved in the management of clinical trial data.
The Technical Accredited Training Program in Clinical Data Management is aimed at further developing essential technical and applied clinical data management skills. The training courses are highly interactive and supported by comprehensive materials and evaluated course work.
This course is aimed at data management professionals who have some hands-on experience across data management or are new to the data management role.
Date: 26th and 27th June 2018
Further details: https://www.acdmglobal.org/training-courses/entry/33/
Hot Topic: 6th July at 12pm (UK time)
eSRA is a free and reliable risk assessment toolkit to help you assess your systems and processes for regulatory compliance.
Why not join us to discuss this intertesting topic, being led by Ioannis Karageorgos from BMS/eClinical Forum and give us your perspective and share your experiences with others across the industry on Friday 6th July 2018@ 12pm BST
This interactive session will be totally FREE of charge to ACDM members and will be around an hour long
Further details: https://www.acdmglobal.org/training-courses/entry/26/
The Association for Professionals in the Management of Clinical Data