Drive innovation across Healthcare Providers, Medical Devices, Pharma and Biotech industries and boost the efficiencies of healthcare eco system operations with high-quality software, engineering, industry domain and talent solutions developed by EZEN .
Potential errors on labels such as:
The labels created for international product delivery, must comply with international regulatory requirements such as FDA, EMEA, MDD and other regional directives per respective regions.
Multiple product identification standards are being used by Life Sciences companies (such as GS1, HIBCC, EAN, & UPC). This needs to be simplified and standardised for products delivered internationally, where they need global supply chain tracking.
In spite of efforts towards global standardisation, there are region specific requirements for products, such as language and regulatory requirements. Local variations of products are applied and verified by corporate and contract manufacturers, suppliers, and distribution facilities.
For Life Science companies, the scope of labelling goes beyond sticking labels. It is a combination of Instructions for Use (IFUs), managing technical and regulatory data, sterilisation and material considerations, etc.




Centralized framework for providing end-to-end Art work creation services as per the specifications and marketing requirements provided by client for all its product packages and labels
Complete Resource Management and job routing at the EZEN Resource Service Center (RSC)
Collaboration across stakeholders i.e., markets and sites for packaging and specification change requirements
Graphic Designers
Proof Readers
Medical Writers
Document Specialists
Validation Engineers
Enlabel
AutoCAD
Adobe InDesign
Corel Draw
Adobe Flash
Adobe Photoshop
Adobe Illustrator
Adobe PageMaker
Loftware