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How to get a marketing authorisation (MA) for an advanced therapy medicinal product (ATMP) so it can be sold and/or supplied in the United Kingdom.
This research seeks to better understand the long-term effects to people in the UK were given human growth hormone extracted from the pituitary gland of people who had died.
A story of hope, medical innovation, and the impact of effective regulation on access to treatment.
Information on comparator products used in studies supporting abridged marketing authorisation application.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Summary: How to get state healthcare if you live, work or study in Bulgaria.
New paper sets out UK regulator's intentions to overhaul rulebook for rare disease therapies in UK
The Human Fertilisation and Embryology Authority (HFEA) oversees the use of gametes and embryos in fertility treatment and research. It licenses fertility clinics and centres carrying out in vitro fertilisation (IVF), other assisted conception procedures and human embryo research. HFEA...
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
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