Date :
Place : Austria, Wien
Contact Person:Andrea Weber
Description:
With the increasing complexity of today’s clinical trials, as well as the speed of technology innovation, unique issues have emerged especially in the area of clinical trials and the use of electronic systems. Understanding regulations – particularly the principles and intent of those regulations – and being able to apply them to new technology and processes in clinical trials is critical to a company’s success. Novel approaches to safeguard data integrity and human subjects need to be considered.Deadline for abstracts/proposals : 27th May 2020
Organized By :Fleming.
Keynote Speakers : Mark Poulton
Conference Highlights :Led by a former GCP Inspector, MHRA, UK with 40 years of experience in the Pharmaceutical Research Industry, Interactive learning approaches, Tailored case studies, Workshop on electronic data issues, Workshop on risk analysis and audit plan for electronic systems, Individual case-by-case consultancy with the trainer, Comprehensive printed and digital course documentation, Certificate of completion issued by the trainer
Check the event website for more details.