69.00€
MedDRA is a Medical Dictionary for Regulatory Authority and it is used by regulatory authorities and the regulated biopharmaceutical industry for data entry, retrieval, evaluation and presentation activities. It is important to understand the basic rules on how to use MedDRA to obtain the most accurate and homogenous data. This course was created both for people who just started their adventure with case management and MedDRA coding, but also for those who want to systematize and expand their knowledge.
What you will learn in this course?
This course contains also a practical part where you check your knowledge and obtain a certificate
Aleksandra is a pharmacist with many years of experience in pharmacovigilance. After graduating, she joined Pfizer as a Junior Safety Data Management Specialist working in the Hub supporting all European countries, Middle East and Africa where she gained experience in case processing activities, triage and acceptance of reports coming from Eudravigilance database and submission to Ethics Committees and Investigators. Currently she manages a team of safety specialists.
Along with her weak spot for the literature cases she is also keenly interested in signal detection.
Passionate about further broadening of her knowledge she regularly participates in numerous trainings, e.g. ‘Signal and Risk Management in Pharmacovigilance MasterClass’ in November 2020, organized by Global Leading Conference, ‘Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors’ in May 2022, postgraduate studies “Management and Monitoring of Clinical Trials” in 2019 at Kozminski University.
Knowing that her work has an impact on health and safety of patients is the greatest motivation and gives her a lot of satisfaction.
When she is not working you can usually meet her cycling or playing squash. She is also interested in learning different languages as they help her to explore new cultures around the world.
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