White Papers

EU MDRS 12 Month Reprieve Thumbnail 300x200 - White Papers EU MDR’s 12 Month Reprieve Posted in: Achieving Regulatory Compliance, Medical Device, Regulatory & Compliance, Whitepaper - Due to Covid-19, on 17th April 2020, the European Parliament gave Medical Device companies a 12-month reprieve on EU MDR.
PRISYM ID Recalls E book 300x200 - White Papers 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 Thumbnail 300x200 - White Papers 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…
EU MDR whitepaper 1 300x200 - White Papers 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 - White Papers 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.
How GUDID Was It For You whitepaper 1 300x200 - White Papers 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 - White Papers 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 - White Papers 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 - White Papers 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…
1 2

EXPLORE OUR RANGE OF RESOURCES