Tag Archives: post-market surveillance

The Role of Regulations in Medical Device Development

: 01-Jan-2025   |   :Kumar Jeetendra

There is no denying that regulations reduce risks in medical devices’ design and development, as well as help to deliver safe and effective marketed products to patients. Medical devices are very much within the purview of regulation as they potentially can affect public health. Regulatory marketing frameworks govern the entire life cycle of the product, […]