DRUG APPROVAL;
DRUG LEGISLATION;
DRUG MARKETING;
DRUG SAFETY;
EUROPEAN UNION;
HERBAL MEDICINE;
HOMEOPATHY;
LICENSING;
PHARMACY;
POLICY;
PRESCRIPTION;
REVIEW;
RISK MANAGEMENT;
UNITED KINGDOM;
ARTICLE;
LEGAL ASPECT;
MARKETING;
DRUG APPROVAL;
GREAT BRITAIN;
LEGISLATION, DRUG;
MARKETING;
MATERIA MEDICA;
PHARMACEUTICAL PREPARATIONS;
PLANT PREPARATIONS;
RISK MANAGEMENT;
Medicines and Healthcare products Regulatory Agency, 2007. A guide to what is a medicinal product: MHRA guidance note no. 8 [online]. Norwich: Her Majesty's Stationery Office. Available: http://www.mhra.gov.uk/home/groups/ comms-ic/documents/publications/con007544.pdf [Accessed 27 March 2009].
Medicines and Healthcare products Regulatory Agency, 2007. A guide to what is a medicinal product: MHRA guidance note no. 8 [online]. Norwich: Her Majesty's Stationery Office. Available: http://www.mhra.gov.uk/home/groups/ comms-ic/documents/publications/con007544.pdf [Accessed 27 March 2009].
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online, Available:, Accessed 27 March 2009
Medicines and Healthcare products Regulatory Agency, 2008. Licensing of medicines [online]. Available: http://www.mhra.gov.uk/howweregulate/ medicines/licensingofmedicines/index.htm [Accessed 27 March 2009].
Development of marketing authorisation procedures for pharmaceuticals
Freemantle N, Hill S Eds, First Edition. Blackwell Publishing and BMJ Books
Irs A et al. Development of marketing authorisation procedures for pharmaceuticals. In: Freemantle N, Hill S (Eds). Evaluating Pharmaceuticals for Health Policy and Reimbursement. First Edition. Blackwell Publishing and BMJ Books, 2004.
Medicines and Healthcare products Regulatory Agency, 2008. Commission on Human Medicines [online]. Available: http://www.mhra.gov.uk/committees/ medicinesadvisorybodies/commissiononhumanmedicines/index.htm[Accessed 27 March 2009].
EudraVigilance, 2009. Risk management for medicinal products in the EU [online]. Available: http://eudravigilance.emea.europa.eu/human/ evriskmanagement.asp [Accessed 27 March 2009].
European Medicines Agency, 2005. Committee for Medicinal Products for Human Use: guideline on risk management systems for medicinal products for human use [online]. Available: http://www.emea.europa.eu/pdfs/human/euleg/ 9626805en.pdf [Accessed 27 March 2009].
European Medicines Agency, 2008. Press release: European Medicines Agency recommends first switch from prescription only to non-prescription for a centrally authorised medicine [online]. http://www.emea.europa.eu/humandocs/ pdfs/epar/alli/4937708en.pdf [Accessed 27 March 2009].
Herbal medicines for menopausal symptoms. DTB 2009; 47: 2-6.
Herbal medicines for menopausal symptoms. DTB 2009; 47: 2-6.
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2004 amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use
European Commission Directive 2004/24/EC of the European Parliament and of the Council of 31 March, Available:, Accessed 27 March 2009
European Commission Directive 2004/24/EC of the European Parliament and of the Council of 31 March 2004 amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use. Official Journal of the European Union [online] 2004; 136: 85-90. Available: http://www.mhra.gov.uk/home/groups/es- herbal/documents/websiteresources/con009359.pdf. [Accessed 27 March 2009].