The Clock is Reset…Opportunity for your Organization to Re-Evaluate compliance to EU MDR Labeling
Jul 15, 2020 10:00 AM EDT, 15:00 PM UK
A webinar from the experts at KPMG & PRISYM ID on meeting the updated timelines for EU MDR
COVID-19, social distancing measures and the obligation felt by the Medical Device industry to prioritize response efforts and reduce any production shortages of necessary supplies to battle this global pandemic, has resulted in the European Parliament voting to delay the implementation of the EU MDR regulation. The European Parliament has officially provided Medical Device Organizations a 12-month reprieve on the European Medical Device Regulation (EU MDR) thus allowing companies the ability and most importantly time in getting their houses in order.
In this webcast, Vishal Pathak, Life Sciences Advisory Manager, Richard Castle, Global Sales Manager Medical Devices at PRISYM ID and Kevin Grygiel, VP Strategic Accounts & Partner Ecosystem at PRISYM ID will delve deeper into the impact of changed EU-MDR timelines and key insights into how the medical device industry will meet labeling and packaging compliance from a Global perspective.
MEET OUR SPEAKERS
Vishal Pathak, Life Sciences Advisory Manager, KPMG
Vishal is a Manager within KPMG’s Advisory Life Science & Core Operations practice. He brings over 10 year of experience related to Supply Chain Operations within the Life Science industry between management consulting and industry roles.
Vishal has recently focused on EU MDR labeling with activities associated from Regulatory down through the Manufacturing Cutover for a Product. He has worked with client cross functional areas to develop strategies for labeling requirements, end to end process improvement, data management and system assessment. He strides to work side by side with the client to bring value, inclusion and innovative solutions to tackle their challenges.
Richard Castle, Global Account Manager Medical Device, PRISYM ID
Having spent most of his career working within the print sector and enterprise level labeling software, Richard is always keen to learn about the regulatory labeling changes the industry faces, like EU MDR, and share his gained knowledge.
Richard is aware of the complex selection process for labeling solutions that customers experience, and he has a proven ability to align their requirements to solutions that are not only valid for today but aligned to any future impact of regulatory changes.
Kevin Grygiel, VP Strategic Accounts & Partner Ecosystem, PRISYM ID
Has over 15 years' experience in software development and implementation helping to deliver complex and personalized business solutions to Life Sciences customers.
Kevin has a proven ability to focus, align and build effective teams with an uncompromising regard for customer impact. He also has the ability to conceptualize, develop and deliver innovative solutions and services that address and resolving enterprise-wide business needs resulting in a high degree of customer loyalty and retention.