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Medical Device Labeling Regulation Changes by FDA for COVID 19 period

FDA is committed to providing timely guidance to support response efforts to this pandemic situation of COVID-19. In…
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FDA/EU/MHRA/TGA Clin monitoring suggestions COVID

There are several suggestions, recommendations from different health authorities for sponsors to handle clinical tri…
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For Labeling Teams, What Does 10 Minutes Saving Per Day Means?

That’s 40 hours time saved per year. The more per day time saving, obviously means more time saved in addition….
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Most Common and Avoidable Mistakes While Adopting ISO 13485

In the process of implementation of QMS standard ISO 13485, many companies face common struggles; however …
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Effectiveness and Flexibility of Adaptive Designs in Clinical Trials

Drug development is becoming a complex process with each passing year. Expenses and time are not at per. Even succes…
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