US FDA

They were of the opinion that the decision to recall was purely voluntary by a few manufacturers A group of doctors from…

Digital diagnosis is now default diagnosis of lab for surgical pathology and 100 per cent of FFPE slides are digitally scanned…

Experts claim ICMR White Paper fails to present balanced overview of risk-benefit ratio of ENDS vis-à-vis other combustible…

The findings establish no endocrine disruption happens from use of PET bottles

Validation of medical devices and its corresponding engineering and manufacturing processes form an integral part of the complete…

The alert by Central Drugs Standard Control Organisation follows US FDA alert flagging these risks

The new catheter from is designed to capture information — such as direction and speed of cardiac signals — often missed with…

The alert mentions three of the five models flagged by US FDA — Astra, Serena CRT-P and Solara CRT-P. Medtronic highlights it…

The technology will ensure faster and accurate diagnosis, thereby improving the quality of life of patients

The facility is 75 per cent automated, boosting annual capacity to over a million units