The Medicines and Healthcare products Regulatory
Agency (MHRA) is reviewing the current system which licences
anthroposophic medicine. The MHRA is the government
agency which is responsible for ensuring that medicines and medical
devices work, and are acceptably safe. The MHRA is an executive
agency of the Department of Health.
You could help us by downloading and individualizing this
letter and approach your MP for help We would be greateful if
you could let us know which
MP or other politician which is open and supportive.
Please follow the link to the MHRA website where
you can download the Review of Medicines Act 1968: Informal
consultation on issues relating to the product licences of right
(PLR) regime and homeopathy
Respones to the informal consultation by
anthroposophic professional and patient organisations;
CAHSC
AHaSC
PAFAM
WELEDA