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End-to-End Solutions for Life Sciences


For companies in the Life Sciences industries, Loftware provides end-to-end solutions that manage the complex processes of creating, managing and printing labels, patient cards, product leaflets and packaging artwork.

life sciences labeling solutions

Manage Complex and Regulated Labeling and Packaging Artwork 

Loftware provides advanced workflow, content management capabilities and certified integrations that together manage the complex processes of creating, managing and printing labels, patient cards, product leaflets and packaging artwork. Loftware offers the only digital platform in the market today delivering a comprehensive solution that helps you improve compliance and accuracy while increasing efficiency and control throughout your supply chain and product life cycle.


Master the Requirements for Medical Device Labeling

Loftware reduces the complexity of life science labeling and streamlines the complete range of medical device labeling processes. Pre-configured, built-in applications automate common labeling operations and enable compliance with regulations such as 21 CFR Part 11, EU MDR and FDA UDI. Data-driven labeling, configurable business logic and advanced workflows help ensure accuracy and consistency.

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labeling regulation compliance software

clinical trial packaging requirements

Transform Your Pharmaceutical Labeling and Packaging Artwork

Improve accuracy and consistency with advanced labeling functionality that integrates with your enterprise applications and supports your serialization process. Loftware supports your efforts to follow Good Manufacturing Processes (GMP) for labels and packaging artwork. Ensure labels and packaging artwork used on your pharmaceutical products include the latest approved content and track changes to labels and digital assets with Loftware’s version control and audit reporting. By automating content selection with configurable business logic, Loftware helps you comply with GS1 standards and meet global regulations such as EU FMD, DSCSA and 21 CFR Part 11.

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Streamline Management of IFUs and eIFUs

Streamline the process for developing, managing and distributing Instructions for Use (IFU) and electronic Instructions for Use (eIFU) with Loftware’s integrated solutions. Loftware helps you reduce waste and improve accuracy for these critical product documents by eliminating fragmented, manual and error-prone tasks and promoting collaboration with internal and external stakeholders. Version control and audit tracking ensure the use of approved content and support regulatory compliance.

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streamline management of IFUs and eIFUs

clinical trial labeling software

Control the Complexity of Clinical Trial Labeling

Ensure accuracy and traceability and eliminate error-prone and time-consuming manual processes with Loftware’s solutions for Clinical Trial Labeling. Automate the management of content, images and translations from the development process through layout, approval and label production with powerful workflow management. Leverage Loftware’s configurable business logic to ensure the right content is included on the right label.

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Meet Compliance and Validation Head-On

Loftware enables you to address expanding regulations, such as EU MDR and IVDR, FDA UDI, along with global labeling standards, such as GS1, efficiently and quickly. With version control and e-Signature capabilities that provide an audit trail of all changes and updates, Loftware empowers you to meet 21 CFR Part 11 requirements. Loftware’s solutions also help you streamline the validation process, reducing costs and speeding the time to validate your labeling.

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clinical testing labeling software

pharmaceutical-labeling-webinar

How One Pharmaceutical Company Optimizes Labeling in SAP

Find out how this pharmaceutical company was able to streamline their labeling processes in SAP, reducing label templates, and improving label management.

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EU MDR White Paper

European Union’s Medical Device Regulation (EU MDR) is clearly a priority for everyone in the medical device industry. As many of you know the enforcement of the first milestone takes effect on May 2020. As the deadline approaches, manufacturers and suppliers are forced to comply with pending changes quickly or be faced with major implications for their business.

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