Does size matter? When it comes to FDA compliance requirements, NO — the FDA does not draw distinctions.
The smallest medical device companies have the same obligations and requirements as companies many times larger, but have to meet them with few resources and within the tightest of budgets. This is particularly an issue when it comes to product labeling and traceability of their devices.
Many smaller companies have met these challenges in innovative ways that work for them at the moment... The problem is this invariably involves manual record keeping, multiple physical copies of labels to prove change control and will inevitably consumes large amounts of time. Time you don’t have.
Technology can help — but it depends on how it is used.
This webinar will help you to understand how a cloud-based SaaS solution could help. You will learn the benefits of this solution, if there are limitations to what it can offer and what the most common commercial models are.
The session will address, among other things:
By the time the webinar is over you will be able to make an informed decision on whether pursuing a cloud-based solutions will work for you.
Register today and sleep easy knowing your days of wasted time and piles of disorganized paper are over.
Who Will Benefit
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VP SaaS Business Development, PRISYM ID
Chris is responsible for development of the PRISYM SaaS solution. Working closely with a Life Sciences focused cloud provider and PRISYM ID’s test and validation experts to deliver a compliance ready solution for small to medium sized companies in the Medical Device sector, Chris manages the SaaS operations team and maintains relationships with customers to ensure on-going feedback and development. With over 25 years’ experience in enterprise software solutions across many sectors, Chris has spent the last 5 implementing and bringing to market SaaS offerings that enable organizations to access high quality services based on leading software technologies.