PMS Reports: Ensuring Ongoing Device Safety
Introduction: Post-Market Surveillance (PMS) is a crucial aspect of the medical device lifecycle, ensuring that devices remain safe and effective even after they have been released to the market. This blog will explore the key components and significance of PMS reports, accompanied by relevant images to enhance understanding. What is a Post-Market Surveillance (PMS) Report? […]
Streamlining Approvals: CDSCO Notice on NSWS Portal Implementation
Welcome to our latest update on the groundbreaking changes in regulatory processes. We are excited to share that the Central Drugs Standard Control Organization (CDSCO) has recently issued a notice, effective January 1, 2024, introducing the National Single Window System (NSWS) Portal. This development aims to revolutionize the approval processes for investors, promoting efficiency and […]
