What happens before a drug enters a “first-in-human” trial?

Ever wondered what preclinical research involves and why is it required?

Karima Benamara shares background information and her personal experience of preclinical writing.

Jane Edwards
Medical Devices Regulation upheaval

The medical device world is facing unprecedented change, global regulations, clinical and technical, the industry has never faced change on this scale. The increased regulatory requirements will affect companies significantly and it is uncertain how many are in a position to deal with the increase in requirements.