This quiz is based on the content from Module 1, Regulation in the UK. The result of this quiz will not count towards your final score.
Select whether the following statements are true or false.
0 of 5 Questions completed
Questions:
You have already completed the quiz before. Hence you can not start it again.
Quiz is loading…
You must sign in or sign up to start the quiz.
You must first complete the following:
0 of 5 Questions answered correctly
Your time:
Time has elapsed
You have reached 0 of 0 point(s), (0)
Earned Point(s): 0 of 0, (0) 0 Essay(s) Pending (Possible Point(s): 0)
MHRA regulates medicines, medical devices, cosmetics, food supplements and blood components for transfusion in the UK.
MHRA’s responsibilities include securing a safe supply chain for medicines and promoting international standardisation and harmonisation.
The Human Medicinal Product and Medical Device Regulations 2014 consolidate UK law concerning medicinal products for human use.
MHRA is responsible for determining whether a product falls within the definition of a medicine as set out in the legislation.
MHRA has the authority to administer and enforce the regulations relating to medicinal products sold, supplied or advertised from within the UK.
Username or Email Address
Password
Remember Me
Username
Email
Registration confirmation will be emailed to you.