medical device
Keeping tabs on Covid-19: MIT engineer paper-based coronavirus diagnostic, Pfizer and BioNTech granted fast track of m-RNA vaccine candidate and FDA issues EUA for nerve device
July 17 by Emily UwemedimoThis week Pharma IQ looks at how the FDA is taking action in the ongoing response effort to fight coronavirus
Medical devices: Rapidly adapting to meet demand in a crisis
July 10 by Billy SiskBilly Sisk, Life Sciences Industry Leader EMEA at Rockwell Automation offers insight into how to start your digital transformation journey to meet market demands during Covid-19
Keeping tabs on Covid-19: Pro bono legal advice offered for vaccine developments, rehydration solution to relieve respiratory symptoms launched and innovative material to protect keyworkers promoted
April 17 by Emily UwemedimoIn a week that saw the UK government announce plans to extend lockdown, Pharma IQ takes a look at some of the actions taken by companies and organizations working in the pharma space to combat Covid-1...
Combination products – A 5 point checklist for compliance approval
July 25 by Chanice HenryAfter a decade in development, products in a multi-billion dollar sector are falling at the last hurdle – under-the-gaze of the regulatorCombination products, or drug and device products, fuse a medic...
The Global Healthcare & Mobile Medical App Development Open Day - Sponsorship Information
October 06 by Pharmaceuticals & Biotechnology EditorOn the 9th December 2014, decision-makers from across the globe will be gathering online to look at successful case studies of how to design, develop and deliver healthcare and mobile apps. The even...
How To: Scalable Unique Device Identification (UDI) Implementation – Real World Lessons Learnt
June 17 by Andrea CharlesThe FDA Final Rule on UDIs is a critical move forward in utilising and leveraging technology to advance medical device information. In this exclusive interview Dawn Fowler, Sr. Manager, Labeling &am...
In Profile: The Top Ten Players in Medical Equipment and Supplies Market
July 20 by Pharma IQPharma IQ provides you with a quick update of the activities of the Top 10 players in medical equipment and supplies market in 2011. Figures according to Forbes The World Biggest Companies.
Conducting Effective Clinical Evaluations for Medical Devices
August 26 by Pharma IQIn this podcast Sven Knoke, Quality and Regulatory Affairs Manager at Siemens, speaks to Andrea Charles from Pharma IQ, about conducting effective clinical evaluations for medical devices and a...
Keeping a Pace with Changes in Clinical Evaluations for Medical Devices
August 26 by Helen WinsorDanielle Giroud, Founder of the World Medical Device Organisation, joins Pharma IQ to discuss regulatory changes in the medical devices market. To listen to the podcast now go to What's Next for...
What's Next for the Medical Devices Market? Regulatory Changes
August 25 by Pharma IQWith the increasing evidence-based medicine politics, the medical device market is changing. In this interview with Helen Winsor from Pharma IQ, Danielle Giroud, Founder of the World Medical Device O...
Balancing Act: Taking a Harmonised Approach to Medical Device Label Interoperability
March 28 by Melissa FinocchioIn this interview Melissa Finocchio, Director, Product Labeling and Documentation BioMerieux, speaks to Andrea Charles from Pharma IQ about changing trends in product labelling and documentatio...
Impact and Implementation: Alere's VP for Regulatory Affairs on the US FDA Unique Device Identification System
March 28 by Simon RichardsAhead of the UDIs and Traceability for Medical Devices Forum 2014, Simon Richards, VP for Regulatory Affairs, EME at Alere, joins Andrea Charles from Pharma IQ to discuss the benefits of a well-buil...