医疗器械

Redefining medical device labeling to meet regulations, control costs, and scale operations in an evolving landscape

100%

W.L. Gore achieves 100% label accuracy

70%

Quest Medical 将标签周转时间缩短了 70%

我们的目标是实施一个集成式标签管理流程,保证标签的准确性和数据的完整性。

Patrick Taels, ICT Manager at Plastiflex Group

标签 support for a healthy supply chain

The medical device industry faces complex supply chain challenges that stem from regulatory shifts, fast moving technological advancements, global market dynamics, and evolving healthcare expectations.

 

To remain competitive and meet these diverse operational hurdles, organizations must focus on product identification. By implementing cloud-based medical label design software, it strengthens traceability, authenticity, and increases connectivity across the supply chain.

Streamline labeling & production

Integrate artwork management and label production for medical devices, secondary packaging, and distribution with speed and accuracy

Enable global compliance

Manage regulations such as FDA 21 CFR Part 11, FDA Unique Device Identification (UDI), and the European Union’s Medical Device Regulations (EU MDR), reducing risks, errors, and fines

Support global & regional labeling

Ensure accurate label localization across languages and symbols, meeting evolving global requirements effortlessly

Track & trace products

Support UDI requirements, recalls, ECG demands, and waste management

Be validation ready

Provide industry-leading documentation, guidance, and support to aid the validation process

Boost supply chain collaboration

Integrate with PLM, MES, and ERP applications as well as any SAP landscape - safeguarding migration to SAP S/4HANA, and supporting supplier/customer connectivity

我们的产品

The right choice
for your business

医疗器械Loftware Cloud Compliance

借助 Loftware 为通过验证做好准备的云标签解决方案,简化您的合规之旅。它专为医疗器械制造商量身定制,无论企业规模如何,都可降低监管风险,加快产品上市时间。

确保可扩展的合规性
效果图管理Loftware Smartflow

通过自动化工作流、内置审批和实时协作,简化您的包装效果图管理。通过 Loftware Smartflow 加快上市时间并确保符合法规要求。

了解 Smartflow 的实际应用

Implanted solutions for your labeling ailments

Staying ahead of compliance challenges

Meeting regulatory labeling and identification compliance on a global scale while addressing regional nuances around language and symbologies is challenging.

 

Medical device manufacturers, co-packers, and suppliers must comply to ensure device integrity, patient safety, market access, and availability worldwide.

 

Loftware’s solutions ensure you meet requirements, ensuring accuracy at every stage of compliance for standards and regulations including:

FDA 21 CFR Part 11

Electronic records and signatures for compliance in labeling

UDI

Identify and track medical devices throughout their lifecycle to improve product safety and streamlining the healthcare supply chain.

EU MDR

Rules that governs the production and distribution of medical devices within the European Union

Health Canada Labeling Requirements

Label content and format standards for Canadian market

GMP Guidelines

Labeling requirements under Good Manufacturing Practice

ISO 13485

Labeling requirements for medical devices and pharma products

China FDA (CFDA) Regulations

Country-specific labeling standards for China

WHO Good Manufacturing Practices (GMP)

Global guidelines for labeling and packaging

Additional resources