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21 Feb 2017 EU Medical Device Regulations – Start preparing NOW!

If you’re not already getting ready for the European Union (EU) Medical Device Regulation change then you should be, according to experts.
After agreement last June between the ‘trilogue’ of the EU Commission, Parliament and Council, the new regulations were published to varied responses from the industry.
With the MDR due to officially come into effect in […]

20 Feb 2017 European Technical Seminar

Visit us in Amsterdam this March.
Anecto will be taking part in the European Technical Seminar at the The Park Inn Hotel, Shiphol Airport, Amsterdam from 9:30 AM – 4:30 PM CET on Wednesday 29 March.
Organised by STERIS, seminar topics will include:

ISO13485: 2016 – top priorities to consider
Business continuity planning
Dose establishment and routine monitoring
Technology comparison
EO residual/cycle […]

08 Feb 2017 Anecto’s authority on ISO 11607

Noel Gibbons will speak about ISO 11607 and packaging validation at the 2017 Med-Tech Innovation Expo in Coventry this April.
Offering an valuable insight into packaging regulations and validation, Anecto’s Lead Programme manager Noel Gibbons will present a talk during this year’s Med-Tech Innovation Expo in Coventry this April 26 & 27.
The talk is titled: ISO 11607 and […]