Wyroby medyczne

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%

Firma Quest Medical skraca czas realizacji etykiet o 70%

Our goal was to implement an integrated label management process that guaranteed accurate labels and data integrity.

Patrick Taels, ICT Manager at Plastiflex Group

Etykietowanie 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

Nasze produkty

The right choice
for your business

Wyroby medyczneLoftware Cloud Compliance

Możesz uprościć proces zapewniania zgodności z przepisami dzięki gotowemu do walidacji rozwiązaniu Loftware do etykietowania w chmurze. Rozwiązanie to, opracowane z myślą o producentach sprzętu medycznego, ogranicza ryzyko regulacyjne i przyspiesza wprowadzanie produktów na rynek, niezależnie od wielkości firmy.

zapewnić skalowalną zgodność
Zarządzanie grafikąLoftware Smartflow

usprawnić zarządzanie projektami opakowań dzięki zautomatyzowanym przepływom pracy, wbudowanym zatwierdzeniom i współpracy w czasie rzeczywistym. Dzięki rozwiązaniu Loftware Smartflow przyspieszysz wprowadzanie produktów na rynek i zapewnisz zgodność z przepisami.

Zobacz rozwiązanie Smartflow w akcji

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:

21 CFR Część 11 FDA

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.

UE 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