Petit-déjeuner : Biological Evaluation of Medical Devices and Healthcare Packaging Testing

Quand :
18 février 2020 @ 9 h 00 min – 11 h 00 min
2020-02-18T09:00:00+01:00
2020-02-18T11:00:00+01:00
Où :
BIOPOLIS
5 avenue du Grand Sablon 38700 La Tronche
Contact :
Linda HAOUCINE
04 76 54 95 63

Come to this session driven by Marcus CORZILIUS, Managing Director for the Life & Health Sciences division at Underwriters Laboratories Inc (UL) in order to understand the progress in biological evaluation and packaging process of Médical Devices.

ISO 11607-1 and ISO 11607-2 recently (2019) have been revised. The presentation is intended to review the key changes and discuss the implications to the validation actions the process of packaging terminally sterilized medical devices:

  • legal basis
  • key changes from first to second edition of ISO 11607-1
  • implications to the validation process
  • shelf life study design examples

ISO 10993-1 has been revised in 2018. The biological evaluation process has been changed and the biological endpoints to be considered have also been revised:

  • Overview of Biological Evaluation Process
  • Upcoming changes to ISO 10993 Parts 3, Part 17 and Part 18

Tuesday 18th February 2020
BIOPILIS
5 avenue du Grand Sablon – 38700 La Tronche
JE M’INSCRIS

Compulsory registration until 14th February 2020 – 1 person/structure

PROGRAMME
From 8h45 : Reception
9h00 – 11h00 : Presentation by Marcus CORZILIUS

Biological evaluation of Medical Devices

  • Review evaluation process per ISO 10993-1 to assess biocompatibility of medical devices
  • Review recent changes to requirements
  • Relevance of chemical characterization
  • Q&A

Healthcare packaging testing

  • Review recent changes to ISO 11607
  • Seal Strength
  • Relevance of usability
  • Q&A

From 11h00 : individual interviews with the speaker

SPEAKER

About Marcus CORZILIUS

Marcus Corzilius is a Managing Director for the Life & Health Sciences division at Underwriters Laboratories Inc. (UL). With a demonstrated history working in public safety, Marcus oversees medical device product safety testing, process improvement (DMAIC), ISO 17025 adherence and GLP oversight. Marcus is a strong business development professional and is recognized thought leader throughout the global safety science industry.

Marcus previously served as a Health Sciences Engineering Leader, an Engineering Manager, and a Project Engineer, leading UL teams on inter-functional teamwork, performance management, and construction review according to medical and laboratory standards.

Prior to joining UL, Marcus worked for five years as a Chemical Laboratory Assistant at Merck and has been a Design Engineer (Surgical Luminaire) for Heraeus. Marcus has his Dipl.-Ing. (FH) in Biomedical Engineering from the University of Applied Sciences in Giessen-Friedberg, Germany and has completed Yale University’s UL Executive Leadership Program. https://www.linkedin.com/in/marcus-corzilius-363b159/?originalSubdomain=de

PARTICIPATION COSTS
MEDICALPS members: free (1 person/structure)
Non-members fees: 60€ (payment by cheque or bank transfer)

CONTACT
Linda HAOUCINE
Communication manager
linda.haoucine@medicalps.eu
0476549563

 

 

 

 

 

 

 

 

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