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Press Releases from Maetrics (9 total)

Maetrics appoints Elizma Parry to lead Clinical Practice

January 2019 – Maetrics, a global leader in life sciences consulting, has appointed Elizma Parry to Director of the Global Clinical Practice. A highly qualified industry professional, Elizma is a proven leader with a strong track record of clinical safety, regulatory and quality management experience. She is leading the company’s clinical practice which is dedicated to delivering effective clinical and performance evidence for international medical device and IVD regulatory compliance.

Maetrics Shine a Spotlight on Clinical Evaluation Reports in the Medical Device …

New Maetrics whitepaper highlights the compliance changes to CERs in light of the new EU Medical Device Regulations and how to navigate them September 2018 – Maetrics, a leading international life sciences regulatory and compliance consultancy, have launched a new report providing clarity to medical device manufacturers on the requirements for properly documented, up-to-date Clinical Evaluation Reports (CER). Correctly implementing the requirements for clinical evaluation is paramount for any manufacturer wishing

Maetrics at Medica 2017: Stand F18-5, Hall 16

Global life sciences consultancy to present original research whitepaper on importance of speedy MDR compliance at Medica 2017 Nottingham, 06 November 2017 – Maetrics, the global consultancy firm that provides regulatory, quality, and compliance solutions to the life sciences sector, today announces its attendance at this 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

Maetrics appoints Brian Moan to European Solutions Delivery Team

15 September 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, Brian is a proven leader with a strong track record in regulatory compliance as well as product quality and design. With over 20 years of experience working with medical device manufacturers, Brian brings extensive industry experience to Maetrics and is ready

Peter Rose divulges ins and outs of new MDR at RAPS Regulatory Convergence 2017

Peter Rose will be discussing the intricacies of the new Medical Device Regulation and providing insight for businesses to ensure seamless compliance at this year’s RAPS Regulatory Convergence 30 August 2017 – Peter Rose, Managing Director for Maetrics operations in Europe and industry leader will be speaking at the upcoming RAPS Regulatory Convergence in Washington DC about the new Medical Device Regulation (MDR) in Europe. The new regulation has consolidated two

Practical checklist of changes to comply with new Medical Device Regulation (MDR …

Maetrics reveals the practical implications for medical device manufacturers and how to address them as the new MDR comes into force June 2017 - Agreement has at last been reached on the new European Medical Device Regulation (MDR), which officially came into effect in May 2017. The new regulation has consolidated two existing legal provisions and replaced both the current Medical Device Directive (93/42/EEC) and the Active Implantable Medical Device Directive

Maetrics launches Swiss seminar series

Maetrics, a global management consulting firm providing life sciences companies with deep quality, compliance, and regulatory solutions has launched a series of training seminars in Basel, Switzerland, as part of its new Seminars and Training Course offering for 2017. The new series of 4 training courses provides added service to client’s continental branches and further cements Maetrics’ position as a global partner. The Risk Management EN ISO14971 course will take place

Maetrics launches NEW Training Courses for 2017

New public and in-house training courses announced Maetrics, a leading global management consulting firm providing life sciences companies with deep quality, compliance, and regulatory solutions has launched its new series of public and in-house training courses for 2017. The independently CPD certified public training courses, provide company staff at all levels of development with key skills to understand the regulatory environment at this time of change. The courses will be held

Are you ready for the fast approaching compliance date for UDI?

Maetrics unveils the current landscape of UDI in the USA and the substantial benefits of early compliance in latest free whitepaper The next imposed compliance date for Unique Device Identification (UDI) in the USA is 24th September 2016 – it could not be more critical, than it is now, for medical device manufacturers to make sure they are prepared. Since 2013, the U.S. Food and Drug Administration have been

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