Dr Marlon Cruz

  • UK Chartered Scientist (CSci)

  • UK Chartered Engineer (CEng)

By - Marlon

Why medical regulatory is important?

Medical regulatory is the process of ensuring that medical products, such as medicines, medical devices and blood components, meet the standards of safety, quality and efficacy before they are placed on the market. Medical regulatory is important for protecting public health and enabling innovation and research that can benefit patients. One aspect of medical regulatory is the classification of medical

Continue reading “Why medical regulatory is important?”
By - Marlon

Medical Devices in UK and EU: the regulatory framework

Medical devices are products or equipment that are used for diagnosis, prevention, monitoring or treatment of diseases, injuries or disabilities. They range from simple bandages and thermometers to complex implants and scanners. Medical devices are subject to strict regulations to ensure their quality, safety and performance. The UK regulatory framework for medical devices originates from EU directives, which were transposed

Continue reading “Medical Devices in UK and EU: the regulatory framework”