Five things Medical Device Industry should expect in 2019

01:00 PM ET | 10:00 AM PT | 12:00 PM CT Duration 90 Minutes

Webinar Includes : All the training handouts , Certificate by the Speaker ,Q/A and 90 Min Live Webinar

"Listen to our expert, Mr. Milind Nadgouda, who is a seasoned quality and regulatory professional with 19 years of industry experience. He is the Co- founder and Director at RiverArk Limited; a Quality Consultancy providing services in GxP space."

What to expect in 2019

Description

The medical device industry makes an enormous number of products ranging from surgical gloves to artificial joints to imaging equipment and plays a crucial role in developing new medical technologies that can improve the ability to diagnose and treat illness.
It’s a market that is very dynamic and The major drivers for the growth of this market are healthcare expenditure, technological development, aging population, and chronic diseases.

Why should you attend:

Emerging trends which have a direct impact on the dynamics of the medical device industry include the changing medical technology landscape, software as a differentiator in medical devices, and design and manufacturing of patient portable and smaller devices.

This webinar will show you the most relevant trends in the industry what will influence the introduction of new products, what impacts will it have on compliance and how will new technology shape the year.

Areas Covered

This webinar will provide the participant with insights on the medical device industry achievements in 2018 and what to expect in 2019. Starting with a background on medical devices trends over the past 3 years; supporting global legislations and some specific emphasis on type of devices.
•         The five key things to expect will be included substantiated with specific reasons why they are important. 
•         The participants will get an understanding of significant impacts to expect on the industry. 
•         The potential challenges that could be expected with the changes occurring on a global level
•         Opportunities that could exist within the industry with emerging technologies and constraints in existing ones
•         Threats that could be perceived by the industry.

Who will Benefit

•         CEO
•         Regulatory VP
•         Quality VPs
•         IT VPs
•         Regulatory Affairs professionals
•         Quality Managers
•         Quality Engineers
•         Small business owners
•         GxP
•         Consultants

Industries who can attend

This 90-minute online course is intended for professionals in the Medical Device, Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.


Speaker Profile

Milind Nadgouda

Milind Nadgouda is a seasoned quality and regulatory professional with 19 years of industry experience. He is the Co- founder and Director at RiverArk Limited; a Quality Consultancy providing services in GxP space. His core areas of specialisation are Risk Strategy (Identification; Assessment; Rating; Prevention and Mitigation); Regulatory Agency Inspection Readiness and Quality Management System GAP analysis. Milind has worked on different types of quality projects with methodologies such Six Sigma; Kaizen and Lean. His expertise on quality strategy and regulatory compliance has been derived from hands on real world experience. So far in his career Milind has been in the frontline during GxP inspections and has on several occasions been in the back room supporting the team for inspections. AstraZeneca, Bristol Myers Squibb, Ranbaxy and Eli Lilly are few of the companies Milind has worked at and consulted. He sees himself as a problem solver and a solution provider.

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