Our Company, Team, Accreditations & Partners
WHAT DRIVES US
The information that must accompany a new drug or a medical device is extensive and complex, and is also highly regulated - because any mistakes or errors can directly affect patient outcomes and patient safety.
Our journey started when a pharmaceutical clinical research team asked us to help them ensure the product data, expiry date, dosage, warning symbols, and every other piece of regulated content required on the labels and leaflets accompanying their clinical trial drugs, were correct when printed.
These small details are critically important, and really matter to every patient or healthcare professional that is relying on any drug or medical device.
So, they really matter to us as well. To the extent that this has been our sole focus for over 15 years.
Which is why, today, our unique products and technologies are being used to deliver certainty that these small details are correct on every one of the 10 million+ medical devices, clinical trial and pharmaceutical products our customers research and manufacture every year.
HOW WE WORK
At PRISYM ID, we strive to collaborate with our customers and users, to understand the pressures they face as they develop and market their products, and their regulatory demands change.
We use our technology and expertise to create innovative products, with a constant focus on how each will help our customers to reduce risk, deliver efficiencies, and ensure compliance.
We also ensure we incorporate the clinical trial, pharmaceutical and medical device best practices we identify into every one of our products, helping all those we work with to benefit from industry leading capability to solve their business problems.
Finally, we take validation and compliance with regulations seriously; it is intrinsic in the products we design, and the processes we use throughout our company. Because we appreciate this is also how our customers are required to operate.
WHAT CAN WE OFFER
PRISYM 360 is designed to specifically address the unique complexities of Medical Device and Life Science labeling and packaging.
It ensures the necessary visibility and control for all aspects of label and packaging artwork design, content and production output, that are essential within this highly regulated industry.
It provides the control and automation of the processes required to create, manage and change approved product content, including the ability to verify and assure the correct approved content is used, to bring certainty.
General ‘enterprise’ software applications offer none of these capabilities, relying instead on manual workarounds to achieve compliance.
PRISYM 360 is provided as a Life Science and Medical Device specific, validated SaaS solution in order to minimize implementation and upgrade effort and, in turn, shorten our customers’ ‘time to value’.
OUR LEADERSHIP TEAM
ISO 9001 ACCREDITATION
As a life sciences organization, you need to be certain we can constantly provide products and services that meet customer and regulatory requirements. The ISO 9001 international standard proves that we have consistent, repeatable processes and achieve operational excellence.
TICK IT PLUS ACCREDITATION
When entering an agreement with a software company, its TickIT Plus certification gives you reassurance that the professional IT practices and quality management is at a consistent level of best practice.
Locations Globally Deployed
Products Labeled Annually
We believe that partnerships are essential to succeed in today's marketplace. We work in a "hands-on" manner with our partners to add real value when implementing Regulated Content and Label Management solutions, so that we can meet our customers’ local, national and international regulatory and compliance requirements.