Improper adverse event reporting acts adversely on medical science
«Missing» or «hidden» data from unpublished clinical trials…
FDA and EMA collaborate on orphan products
Rare diseases affect about 60 millions of people in EU and the…
X7 Research at CPhI 2016
4-6 October 2016 - X7 Research participates in global conference…
FDA attempts to achive uniformity in registration dossiers for medical devices
FDA announced the availability of the final guidance entitled…
“Real world evidence” clinical trials – paradigm shift in clinical research?
Results obtained from clinical trials usually have limited relevance…
Course: "Good Clinical Practice"
Dear colleagues!
Let me invite your employees on a regular…