Maetrics Ltd of Nottingham at MEDICA 2017 in Düsseldorf -- MEDICA Trade Fair
Premium Exhibitor

Maetrics Ltd

BioCity Nottingham, Pennyfoot Street, NG1 1GF Nottingham
United Kingdom of Great Britain and Northern Ireland

Telephone +44 115 9216200
infoeurope@maetrics.com

This company is co-exhibitor of
ABHI Association of British Healthcare Industries Ltd.

Hall map

MEDICA 2017 hall map (Hall 16): stand F18-5

Fairground map

MEDICA 2017 fairground map: Hall 16

Contact

Peter Rose

Managing Director, Europe

Phone
0044 115 921 6200

Our range of products

Product categories

  • 07  Medical Services and Publications
  • 07.08  Logistic services
  • 07  Medical Services and Publications
  • 07.08  Logistic services
  • 07.08.06  Consulting for health organisations

Consulting for health organisations

  • 07  Medical Services and Publications
  • 07.08  Logistic services
  • 07.08.14  Process analyses
  • 07  Medical Services and Publications
  • 07.10  Technical equipment management, Test houses / Certification Bodies

Technical equipment management, Test houses / Certification Bodies

  • 07  Medical Services and Publications
  • 07.10  Technical equipment management, Test houses / Certification Bodies
  • 07.10.02  Certification and testing of medical devices, quality assurance

Certification and testing of medical devices, quality assurance

Our products

Product category: Logistic services, Consulting for health organisations, Process analyses, Technical equipment management, Test houses / Certification Bodies, Certification and testing of medical devices, quality assurance

Maetrics - compliance and regulatory solutions

Maetrics offers its unique insight and experience as a leading regulatory and compliance consultancy. With offices in Basel (Swizerland) and Nottingham (UK), we can support your team on the ground, helping your company meet  regulatory requirements and drive business improvements. 

OUR SERVICES

1. Regulatory Compliance
2.  Quality Management Systems Strategies
3.  Validation
4.  Clinical Evaluation Reports
5.  Product Life Cycle Risk Management
6.  Performance Improvement
7.  Project & Program Management
8.   M & A Integration & Support
9.    Training
10.  Information Technology
11.  Data Analysis & Reporting 

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Company news

Date

Topic

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Oct 31, 2017

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

Maetrics, the global consultancy firm that provides regulatory, quality, and compliance solutions to the life sciences sector, today announces its attendance at 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 medical devices sector. To coincide with the event, Maetrics will also launch a new research whitepaper on the European Medical Device Regulation (MDR), which officially came into effect in May this year and represents the single largest change to medical device regulations in Europe since CE Marking was introduced in 1993.

Specifically, the original research will quantify in clear financial terms the potential market advantage for medtech firms moving quickly to become compliant with the MDR, rather than waiting until the 2020 deadline. 

Peter Rose, Managing Director for Europe at Maetrics, said: “We are delighted to exhibit at this year’s Medica and look forward to presenting our significant knowledge of the medical devices regulatory landscape.  There are significant changes taking place that widely affect the industry – including the MDR in Europe, the new international Medical Device Single Audit Program (MDSAP) and ISO 13485:2016.

“Based on our current experience of helping medical device companies navigate these important regulatory changes and meet their obligations, we are ideally positioned to give insight into the practical implications of each regulation and the tactics being employed to achieve seamless compliance.”

Maetrics works with medical device, diagnostic, pharmaceutical and biotechnology companies to help them meet quality, compliance, and regulatory requirements while remaining competitive and profitable. With offices throughout Europe and North America, Maetrics can assist with local, regional, or global compliance needs.

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Notes to Editors

Peter Rose – biography
Mr. Rose has worked in the medical device industry for over 24 years, bringing a wealth of experience and knowledge in quality systems and regulatory affairs to Maetrics’ clients. He is a lead auditor and a qualified microbiologist, and has been recognized for his extensive experience with sterilization. In addition to his Maetrics responsibilities, Mr. Rose is also a Director of Medilink East Midlands and has been a guest lecturer at the University of Nottingham, Nottingham Trent University and the University of Sheffield. He is a member of the Technical Policy Group of the ABHI and sits on the MHRA Medical Device Industry Liaison Group. He is a contributor to a number of industry journals and is sought out regularly to speak on industry topics. Mr. Rose is a graduate of the University of Sheffield -BSc (Hons) Degree in Microbiology.

About Maetrics
Founded in 1984, Maetrics is a global life sciences consulting firm focused exclusively on regulatory, quality, and compliance solutions for Medical Device, Diagnostic, Pharmaceutical and Biotechnology companies.  With offices throughout Europe and North America, Maetrics can assist with local, regional, or global compliance needs.

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About us

Company details

Founded in 1984, Maetrics is a global consulting firm dedicated to guiding life sciences companies through the successful management of quality, regulatory, and compliance strategies.

With offices throughout Europe and North America, Maetrics offers more than theory. We deliver actionable, practical, and realistic strategies designed to fit a client’s needs. Our knowledge, experience, and collected talent drive our ability to effectively evaluate client operations, identify areas for improvement, and execute customized plans. Our consultants and industry leaders implement comprehensive quality, compliance, and regulatory solutions that allow clients to remain competitive and profitable.

EXPERIENCE MATTERS

It takes knowledge and experience across many disciplines to effectively manage regulatory compliance. Our consultants combine risk-based quality management methods, project management tools, program management, and industry best practices to maintain regulatory, quality, validation, and engineering compliance.

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