Blogs
Medical Devices – USA/Europe Regulato…
EUROPE Commission Implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for t…
MHRA Guidance on the use of Real-Worl…
There are vast amounts of data being collected on patients, for example, in electronic health records…
Procedural Aspects for the Consultati…
The guidance document aims to provide interested parties in particular notified bodies, device manufa…
Medical Device Patient Information Le…
From 1st December 2021, all Implantable and Active Implantable Medical Devices (AIMD) are required to…
Anti-Infective Drug Products for the …
The US Food and Drug Administration (FDA) issued final guidance to assist sponsors in developing anti…
Medical Devices–Asia Regulatory Updat…
Japan(PMDA)
MHLW Pharmaceuticals and Medical Devices Safety Information (FY2021) No. 387
At t…
Don’t miss out! Click here to stay in touch.
Categories
Most used Tags
CONNECT WITH US
The First Step
Let's talk about how Vistaar can help you