AAMI Webinar on HFE Reports for Medical Device Manufacturers
March 15, 2018
By Neozene

A new webinar hosted by the Association for the Advancement of Medical Instruments (AAMI) will provide insights into preparing Human Factors Engineering (HFE) test plans and reports that existing regulatory guidance does not fully address. The AAMI webinar, “Writing Human Factors Plans and Reports,” has been developed to cover the lack of sample work products in HFE guidance documents issued by the US Food and Drug Administration and other regulators. The webinar takes place March 15, 2018 at 11am Eastern US time. Topics the webinar will cover include: HFE project plans

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Why Clinical Trial Support is Important!
February 13, 2018
By Neozene

Clinical trials are a key research tool for advancing medical knowledge and patient care. Clinical research is done only if doctors don’t know: whether a new approach works well in people and is safe and which treatments or strategies work best for certain illnesses or groups of people. Some clinical trials show a positive result. For example, the National Heart, Lung, and Blood Institute (NHLBI) sponsored a trial of two different combinations of asthma treatments. The trial found that one of the combinations worked much better than the other for

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4 Advantages of Working with a Clinical Trial Research Organization
September 5, 2017
By Neozene

Here are 4 advantages of using a CRO in your clinical trials: By using a CRO you can avoid having to spend capital on human resources or equipment your organization may not already have.  If your pharmaceutical or healthcare organization is not experienced at carrying out clinical trials, the chances are that to successfully complete one you will have to invest in more resources – whether that be more staff, more equipment or something else. If you engage a CRO to work with you will save your organization from having to do this.

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