Join us as we learn about the newest changes at the FDA since January 1, 2017; hear a panel discuss the challenges and special efforts that are being made in the world of Cyber Security, and listen to some of the newest adventures into Regenerative Medicine being made that will affect many of our companies and products in the future.
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The European Union Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) came into effect as of May 26th, 2017. The clock is ticking for current Medical Device manufacturers in the European marketplace to develop and implement strategies to be fully compliant. The new In Vitro Diagnostic Regulation (IVDR) is complex and the […]January 26, 2018
While pharmaceutical companies are ultimately responsible for assuring the control and review of outsourced activities and the quality of purchased materials, many struggle with supply chain visibility due to the complexity of multi-tiered supply chains, inadequate IT systems, limited experience, and resource constraints. This ebook, created by Generis in partnership with Maetrics, addresses: Why manufacturers […]November 22, 2017
In this new research paper, Maetrics details the $16.5BN competitive market advantage for medtech firms that move quickly to comply with the new European Medical Device Regulation (MDR). The MDR is designed to improve both clinical safety and fair market access for all medtech players, but a rapidly emerging capacity shortage both among Notified […]November 17, 2017
Maetrics, the global consultancy firm that provides regulatory, quality, and compliance solutions to the life sciences sector, has published a free step-by-step whitepaper to help manufacturers understand the imminent changes and how to comply with the new IVDR that repeals Directive 98/79/EC as well as Commission Decision 2010/227/EU. To get a real handle on the major […]January 30, 2018
Maetrics, the global consultancy firm that provides regulatory, quality, and compliance solutions to the life sciences sector, will attend next month’s Medica trade fair in Düsseldorf (13-16 November 2017). The company will exhibit on Stand F18-5, Hall 16 and will have senior executives available to share their experience and expertise in regulatory affairs in the […]October 26, 2017
UK (September 04, 2017) – Maetrics, a global leader in life science consulting, has appointed Brian Moan to Director of Solutions Delivery in Europe. A highly qualified industry expert and thought leader specializing in Human Factors, Brian has been involved in MHRA working groups to develop industry guidance, has frequently presented around regulatory issues and has developed […]September 19, 2017
We are delighted to invite you all to attend and register for the “7th International conference on Pharmaceutical Auditing (Pharma Audit 2018) which is going to be held during June 06-07, 2018 at Philadelphia, USA. Our Director of Solutions Development, Jennifer Lopez will be presenting on Maximizing the Impact of Strong Compliance Audits. For more […]February 22, 2018
MEDICA is the world’s largest event for the medical sector. For more than 40 years it has been firmly established on every expert’s calendar. There are many reasons why MEDICA is so unique. Firstly, the event is the largest medical trade fair in the world – in 2016 it attracted more than 5,100 exhibitors from 70 countries […]October 3, 2017
Join us as we learn about the newest changes at the FDA since January 1, 2017; hear a panel discuss the challenges and special efforts that are being made in the world of Cyber Security, and listen to some of the newest adventures into Regenerative Medicine being made that will affect many of our companies […]October 3, 2017