Blogs
Medical Device Post Market Surveillance
The post-market surveillance (PMS) systems that monitor medical device safety after launch reduce bot…
Why is Medical Technology Getting Shr…
Cybersecurity threats top the list when it comes to imminent dangers surrounding the healthcare indus…
Labeling Requirements for Medical Dev…
Labeling acquires a major part when it comes to ensuring the safety of those that are using it. The l…
IMDRF Offers Final Clinical Guidelines
The International Medical Device Regulators Forum (IMDRF) released three final documents covering cli…
South Africa released Guidelines R…
The South African Health Products Regulatory Authority (SAPHRA) invites applicants to submit Expressi…
USA: FDA Modifies List of Standards f…
The US Food and Drug Administration (FDA) modified the list of standards to assist medical device man…
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