As the FDA continues to develop and solidify its guidance and regulations on AI, medical device manufacturers should prepare ...

The medical device industry faces unique challenges as PFAS begins to face regulation in the U.S. and Europe despite ...

The FDA categorizes medical devices into three classes, namely Class I, Class II, and Class III. Regulatory control increases from Class I to Class III. 1 The agency has classified approximately ...

Centre notifies rules for recruitment of medical device officers in CDSCO: Gireesh Babu, New Delhi Monday, November 11, 2024, 08:00 Hrs [IST] In an effort to strengthen the regula ...

PharmaReg and MedDevReg AfriSummit host 80+ regional and international speakers alongside over 300 pharmaceutical and medical ...

Dr. Najiba Al Shezawy, Co-Chairman of AfriSummit, expressed her gratitude for the participation of African National ...

Evolus (EOLS) announced the EU Medical Device Regulation certification was received for four unique injectable hyaluronic acid gels under the ...

Quantiphi Global Head of Healthcare and Life Sciences Barinder Marhok said the partnership marries DDReg’s expertise in ...

The core responsibility of regulatory affairs is to ensure products meet safety and quality standards from development to ...

Targets the reduction in CABG-related bleeding severity due to the blood thinning drug, ticagrelor – a major unmet medical need in heart attack ...

The parliamentary resolution drew the immediate support of MedTech Europe and VDGH, but it remains unclear what the immediate ...

today announced the EU Medical Device Regulation (MDR) certification was received for four unique injectable hyaluronic acid (HA) gels under the brand name Estyme ® (pronounced "esteem"), branded ...