Advances and developments in data use in pharmacovigilance are driving new training needs and demands. The sheer volume of data, along with the enforcement of new ISO standards for Individual Case Safety Reports, have created a pressing need for industry best practices to cover numerous aspects of working the data. These include data entry conventions, management data, quality assurance and preparing to work with AI tools, all within the limitations imposed by the EU GDPR.
Swiss Biotech Members receive 15% discount from the registration fee.
June 8, 2021 @ 2:00 pm
June 10, 2021
Virtual Event
101
Days15
Hours13
MinutesVirtual Event