Good clinical practice (GCP) provides guidelines for designing, conducting, recording, and reporting clinical trials that involve human participants. GCP sets standards that need to be followed by conducting clinical trials. It ensures that the rights, safety, and...
In this blog, we have discussed common medical device industry quality challenges. Additionally, we have provided some tips on how to overcome them. What are medical device industry quality challenges? Medical device industry quality challenges are technical,...
Clinical chemistry reagents and kits are considered in-vitro diagnostic devices (IVDs) per CDSCO guidelines. They are regulated by the Medical Device Rules, 2017. To manufacture or import clinical chemistry reagents and kits, you need to comply with CDSCO...
With growing healthcare infrastructure and increasing demand for advanced medical technologies, the Indian medical device market provides considerable opportunities. India’s healthcare sector is one of the fastest-growing industries, with the medical device market...
Medical devices form the backbone of the healthcare industry. They are constantly being used to diagnose, treat, and monitor patients. The medical device industry is a dynamic sector buzzing with new investment opportunities. We have highlighted some key medical...