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(University of Maryland School of Medicine) The GammaPod -- a first-of-its kind stereotactic radiotherapy system to treat early stage breast cancer -- has received 510(k) clearance from the US Food and Drug Administration (FDA), paving the way for the manufacturer to bring the system to market for the treatment of breast cancer patients.NEXT ARTICLE
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In order to become availible to pateints, drugs need to undergo a number of phases of clinical trials to test their efficacy and safty and to then be authorised by the drug approval organistion in each respective country. This is the FDA in the USA and N...