Ethics in clinical research evolves
For the first time since it was issued in 1991, the Common Rule…
Pharmacovigilance market grows with implementation of new regulatory requirements
The rise in the prevalence of acute and chronic diseases leads…
Prospective medical device safety surveillance: role of tracking and databases
Medical device manufacturers should track and report device malfunctions,…
When there is no choice – EMA and FDA allow early access to market for indispensable medications
Current regulations in drug development field assume complicated…
Advanced Training Course
The advanced training course for professionals – The…
Educational program “Good Clinical Practice”
Educational program “Good Clinical Practice” – a course…