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Adverse Reaction Reporting Guide for …
New Zealand tends to have a high rate when it comes to adverse reaction reporting. The Centre for Adv…
Unique Device Identification System
The FDA established the unique device identification system to adequately identify medical devices so…
FDA Warning Letter Jan-Apr 2021 Recap…
Warning DescriptionProducts & SummaryFDA has seen manufacturer’s Website and their claims on prod…
Labeling Requirements for Prescriptio…
Under FDA there are more than 150 labeling resources that are present for labeling prescription drugs…
Medical Device Labeling under FDA
Food and Drug Administration (FDA) puts forth certain regulations in the U.S. that are abiding on foo…
EU Regulations: Things Still to be known
Medical Device Regulations (EU) 2017/745 is an advancement that would help EU in coping with medical …
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