Regulatory authorities around the world are moving toward electronic product information (ePI) built on FHIR®. But with so many acronyms, formats, and evolving requirements, it can be hard to keep up. That’s why we created FHIR ePI 101: A Beginner’s Guide to Electronic Labeling.
E-labeling is no longer on the horizon – it’s here. That’s why we created this playbook: a one-stop resource combining expert insights, survey data, and practical guidance for life sciences professionals.
How to Ensure Barcode Accuracy in a Fast-Moving Market: Barcodes are the backbone of traceability, compliance, and retail readiness. But in today’s digital-first design workflows, traditional print-based grading methods no longer tell the full story.
As regulatory bodies move toward structured electronic product information (ePI) in FHIR XML format, life sciences organizations are under pressure to evolve. That includes how you verify and proofread content.
Practical next steps for pharmaceutical manufacturers & distributors as regulators demand the digital delivery of customer-facing product information in place of paper inserts.
Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.
Managing medical device labels presents a myriad of challenges for manufacturers, including ensuring compliance with ever-evolving regulatory standards, maintaining accuracy and consistency in label content, and optimizing label design for clarity and usability.
As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing. But how well prepared are suppliers? We recently commissioned independent research to find out.
Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?
Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors
