Medical device manufacturers face the challenge of efficiently managing increasingly high volumes of data relevant to product labeling in a vast array of different forms.
Category Archives: Achieving Regulatory Compliance
Why Medical Device Manufacturers Must Look at the Bigger Picture When Implementing a GLS
What is Annex VI EU No 536/2014 and how does it affect Labeling?
Why a Global Labeling System is becoming critical for Medical Device Manufacturers
11TH ANNUAL MEDICAL DEVICE & DIAGNOSTIC LABELING CONFERENCE
PRISYM ID BOOSTS CUSTOMER SERVICE OFFER WITH NEW CUSTOMER EXPERIENCE TEAM
PRISYM ID joins Siemens Digital Industries Software Solution Partner Program as a Software and Technology Partner
PRISYM ID underlines its commitment to patient safety with updated GS1 certification
PRISYM ID announces six further projects go live as medical device and life science organizations prepare for the future
COVID LEGACY: A New Era For Clinical Trials?
In the last fifteen months both individuals and organizations have had to change their behaviors. It’s typically meant more activity being done remotely, requiring greater agility and pace to deliver against changing demand, with technology often being deployed to overcome the unique challenges the pandemic has posed.