by Syrma Johari | Sep 1, 2022 | Medical Device, Regulatory
Risk Management in Medical Devices is a complex process and requires a strategic approach requiring careful analysis of steps involved in the manufacturing process. ISO 14971 requires specific practices meant for strategically implementing risk management in a Medical...
by Syrma Johari | Aug 22, 2022 | Medical Device
Change is an essential part of the Medical Device Development Process. Every successful Medical Device starts from a naïve idea that undergoes very rigorous processing to come out as a successful medical device serving an exact purpose. A Medical Device Development...
by Syrma Johari | Aug 19, 2022 | Medical Device
Medical Device Development is a multilevel process. Each step needs strict monitoring and documentation. But why document everything? Is it just because Medical Devices deal with human lives? Yes, it is! Not only it is a necessary practice for end-user’s safety but...
by Syrma Johari | Aug 18, 2022 | Medical Device
The success of the Medical Device depends on the level of impact it creates. With an ever-growing population, the need for accessible, accurate, and affordable diagnostics is increasing. Here we discuss how AI-based Diagnostic devices make lives easier and treatment...
by Syrma Johari | Aug 10, 2022 | Medical Device
The Medical Imaging Market was USD 36.19 billion in 2020 and it is estimated reach USD 56.53 billion by 2028, exhibiting a CAGR of 5.8%. The optical imaging market on the other hand will reach USD 3.3 billion by 2026 from USD 1.6 billion in 2021 at a CAGR of 14.8%....
