Blogs

eLearning Project Managment

Ensure Your eLearning Project Stays on Track

Whether you are launching an eLearning project for a non-government organization (NGO) or a corporation, your project can quickly become derailed without proper planning and management. For learning and development (L&D) and eLearning professionals across industries, an eLearning project launch requires foresight, planning, and expert project management. From the very onset, a successful eLearning project […]

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Professional Staffing Solutions

Why Work With a Professional Staffing Solutions Company?

eLearning Staffing Challenges in an Ever-evolving Recruitment Landscape “Fifty-five percent… of owners reported few or no qualified applicants for the positions they were trying to fill.” — NFIB¹ Looking for high-level candidates with the relevant experience and expertise with today’s eLearning strategies, tools, and techniques? Then you are not alone. From life sciences and healthcare

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Glossaries and Termbase for Life Sciences Industry

Terminology Management for Life Sciences

Glossaries and Termbases for Medical Device Companies As social, political, and economic ideologies shift and evolve throughout the world, so too do terms, acronyms, and phrases within businesses and across industries. And, as the world continues to globalize, these terms, acronyms, and phrases must now be accurately translated into multiple languages to ensure effective communication

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Software UI Localization For the Life Sciences Industry

Software Localization for the Life Sciences Industry

Software Localization Impacts The User Experience Life sciences software localization requires much more than simply checking off a list of requirements in a regulatory box. As the title suggests, this specialized type of localization ensures that your device’s user interface is accurately localized for each intended market. The success of your medical device is intricately

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In-Virto Device Regulation

Ready or Not – Here comes IVDR

The European Union’s new regulation for in-vitro medical devices, 2017/746 (IVDR), takes effect in May 2022. While IVDR aims to increase patient safety and company transparency, it also creates heightened challenges for the entire supply chain (especially for in-vitro diagnostic companies and their medical safety program managers). In its most recent report, the European Commission

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