White Papers

PRISYM ID Recalls E-book How to Avoid Four Common Labeling Product Recalls Posted in: Achieving Regulatory Compliance, Increasing The Operational Efficiency, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper - Companies’ continued reliance on manual processes and disparate labeling systems often culminates in pricey product recalls.
PRISYM ID 10 Steps to EU MDR Labeling Implementation Guide 10 Steps to EU MDR Labeling Implementation Posted in: Achieving Regulatory Compliance, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper - Whether you’re producing medical devices within Europe or supplying to Europe, as a manufacturer or supplier, you will need to…
Developing 2020 Vision Will Your Labeling Strategy Assure Compliance with EU MDR Developing 2020 Vision: Will Your Labeling Strategy Assure Compliance with EU MDR? Posted in: Achieving Regulatory Compliance, Medical Device, Regulatory & Compliance, Whitepaper - The European medical device industry is a third of the way into a 3-year transitional period that will culminate with…
EU MDR whitepaper 1 300x200 - EU MDR Labeling Compliance: Learning The Lessons From UDI EU MDR Labeling Compliance: Learning The Lessons From UDI Posted in: Achieving Regulatory Compliance, Business Analysis, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper - The European medical device industry is in the grip of the biggest changes the market has seen in decades.
Mind Your Language whitepaper 1 300x200 - Mind Your Language! Requirements for Local Language Labeling in Clinical Trials Mind Your Language! Requirements for Local Language Labeling in Clinical Trials Posted in: Achieving Regulatory Compliance, Clinical Trials, Operations & Labeling, Regulatory & Compliance, Whitepaper - Global clinical trials labeling can be a complex subject and is an integral part of clinical trials supplies management. The…
How GUDID Was It For You whitepaper 1 300x200 - How the GUDID was it for you? How the GUDID was it for you? Posted in: Achieving Regulatory Compliance, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper - An examination of UDI implementation and lessons for manufacturers of Class II device. Almost two and a half years after the…
Validation whitepaper 1 300x200 - Validation; Business Gain Without the Pain Validation; Business Gain Without the Pain Posted in: Achieving Regulatory Compliance, Business Analysis, Medical Device, Project Managers, Regulatory & Compliance, Whitepaper - How leveraging supplier validation capabilities can help transform the validation cycle and drive progress, productivity and profitability.
Delaying Tactics whitepaper 2 300x200 - Delaying Tactics - How a Postponement Strategy can transform Documentation Processes and bring Supply Chain Agility Delaying Tactics – How a Postponement Strategy can transform Documentation Processes and bring Supply Chain Agility Posted in: Business Analysis, Clinical Trials, Increasing The Operational Efficiency, Operations & Labeling, Supply Chain, Whitepaper - The introduction of Unique Device Identification (UDI)regulations signals a seismic shift in theMaintaining an efficient supply chain is widely acknowledged…
Aligning For Growth whitepaper 2 300x200 - Aligning For Growth: The Evolution Of Medical Device Labeling Aligning For Growth: The Evolution Of Medical Device Labeling Posted in: Assisting With The Consolidation, Business Analysis, Enabling the Expansion, Medical Device, Operations & Labeling, Supply Chain, Whitepaper - The introduction of Unique Device Identification (UDI)regulations signals a seismic shift in the labeling of medical devices. Over the past…
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