UK Parliament / Open data

Medicines and Medical Devices Safety Review

The simple answer to that question is yes: there are legal consequences for regulators who have failed. In that instance, it would be the responsibility of the Government, or of the drugs companies who failed in their responsibility to inform patients of the dangers of taking drugs. The priority is to establish the facts. Some of those are clear now, but some are not, and that is why I think that the review will help us.

Type
Proceeding contribution
Reference
636 c174 
Session
2017-19
Chamber / Committee
House of Commons chamber
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