Maetrics Launches NEW 2016 Seminars & Training Courses Schedule
Maetrics
-
global
international consulting firm providing life sciences companies with deep quality,
compliance and regulatory solutions
–
has launched
its new Seminars and Training C
ourse
s
schedule
for 2016. Highlights this year include the introduction of half day seminar
s as well as a unique one
day course on EU and US Design Control Requirements.
Maetrics ’ half day se minars are designed for executives, directors and high level managers with the aim to provide an overview of information of best practice on topical quali ty and regulatory issues. Maetrics will provide insight from manufacturers, regulators and competent authorities to help ensure attendees can appropriately plan, budget and prepare their business in the ever - changing regulatory environment.
Upcoming Maetrics seminars in 2016 (in London):
? The new IVDR and the effect on manufacturers – 21 April 2016
? The changing climate of CERs – 08 June 2016
? The new MDR (Medical Device R egulation) and the effect on manufacturers – 27 September 2016
? Changes to EN ISO 13485 – quality management systems for medical devices – 20 October 2016
Upcoming Maetrics seminars in 2016 (in Leeds):
? Changes to EN ISO 13485 – quality management systems for medical devices – 25 May 2016
? The new IVDR and the effect on manufacturers – 05 October 2016
? The changing climate of CERs – 05 December 2016
Maetrics also offer a wide range of public training courses delivered by experienced Maetrics trainers who understand the needs of professionals in the medical device, pharmac eutical and bi otech industries. All Maetrics training courses are CPD certified and will be held in Birmingham.
Upcoming training courses in 2016 include: CE Marking and 93/42/EEC; Creating a technical file/design dossier; Risk management EN ISE 14971; Usability and h uman factors and electrical medical equipment; Post market surveillance and adverse event reporting; Clinical evaluations reports; Medical device software and mobile apps; Process validation – IQ,OQ,PQ; EU and US design control requirements; EN ISO 13485 internal auditor.
Pete Rose, Managing Director at Maetrics, Europe, says: “As an extension of our broad service portfolio exclusive to regulatory, quality and compliance within the life sciences industries, we are excited to offer the new seminars and tr aining courses”.
He continues: “Our training courses are suited to beginners, those who require bringing up to date with new developments and those who need a refresher. Our classes teach real - life strategies and solutions that can be applied to any life sciences organisation.”
V isit www.maetrics.co.uk for more information or contact us on +44 (0)115 921 6200
Maetrics ’ half day se minars are designed for executives, directors and high level managers with the aim to provide an overview of information of best practice on topical quali ty and regulatory issues. Maetrics will provide insight from manufacturers, regulators and competent authorities to help ensure attendees can appropriately plan, budget and prepare their business in the ever - changing regulatory environment.
Upcoming Maetrics seminars in 2016 (in London):
? The new IVDR and the effect on manufacturers – 21 April 2016
? The changing climate of CERs – 08 June 2016
? The new MDR (Medical Device R egulation) and the effect on manufacturers – 27 September 2016
? Changes to EN ISO 13485 – quality management systems for medical devices – 20 October 2016
Upcoming Maetrics seminars in 2016 (in Leeds):
? Changes to EN ISO 13485 – quality management systems for medical devices – 25 May 2016
? The new IVDR and the effect on manufacturers – 05 October 2016
? The changing climate of CERs – 05 December 2016
Maetrics also offer a wide range of public training courses delivered by experienced Maetrics trainers who understand the needs of professionals in the medical device, pharmac eutical and bi otech industries. All Maetrics training courses are CPD certified and will be held in Birmingham.
Upcoming training courses in 2016 include: CE Marking and 93/42/EEC; Creating a technical file/design dossier; Risk management EN ISE 14971; Usability and h uman factors and electrical medical equipment; Post market surveillance and adverse event reporting; Clinical evaluations reports; Medical device software and mobile apps; Process validation – IQ,OQ,PQ; EU and US design control requirements; EN ISO 13485 internal auditor.
Pete Rose, Managing Director at Maetrics, Europe, says: “As an extension of our broad service portfolio exclusive to regulatory, quality and compliance within the life sciences industries, we are excited to offer the new seminars and tr aining courses”.
He continues: “Our training courses are suited to beginners, those who require bringing up to date with new developments and those who need a refresher. Our classes teach real - life strategies and solutions that can be applied to any life sciences organisation.”
V isit www.maetrics.co.uk for more information or contact us on +44 (0)115 921 6200