CPHI Online is the largest global marketplace in the pharma ingredients industry
Managing risks in pharmaceutical and healthcare labeling
Pharmaceutical and healthcare packaging labels play a critical role in a drug or medicine’s journey from manufacturing to patient administration. Watch our webinar to learn more about how to proactively manage the risks that come with selecting pharma labeling. You will learn more about:
- The effects of using standard labels vs pharmaceutical grade labels
- Regulatory compliance
- Supply security and second specification
2016On CPHI since
1000 - 4999Employees
Other Content from UPM Raflatac (2)
How can label choices enhance packaging sustainability?Patient safety and regulations have been the key drivers for the design of pharmaceutical packaging materials, but there is a growing need for the industry to ensure that packaging is also environmentally sustainable.
Packaging sustainability can be improved through two key ways. Switching to reduced, recycled and renewable label materials and choosing label solutions that support packaging recyclability and reuse.
Download the guide and learn how to meet corporate sustainability targets without compromising product safety or functionality.
In the sustainable pharmaceutical labeling guide:- Recycling of pharmaceutical packages
- Label recommendations for different packaging types
- Innovative labeling materials that can help ensure your packaging is environmentally sustainable
- Services that help you optimize your labels for a smarter future beyond fossils
Low-performance labels that create leachable chemical compounds may fail testing or perform poorly across your pharmaceutical product’s lifecycle, resulting in significant launch delays or costly recalls.
This white paper created by pharmaceutical packaging experts walks you through the key steps in ensuring migration-safe packaging and labels.
Learn in this comprehensive white paper:
What is primary, secondary, and tertiary pharmaceutical packaging?
Glass vs. plastic packaging - what are the pros & cons?
What key regulations for pharmaceutical packaging must I take into account?
How and why can label materials leach into packaging forms?
What drug packaging does the FDA classify as high-risk for leaching?
How can I streamline packaging testing to speed up product launches?
What industry best practices should I adhere to, such as change management procedures?
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