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Are you lost in the deep space of version control? The answer is probably yes if you are still managing your artwork manually through emails, spreadsheets, and disparate tools.But we have good news! You don’t have to be a giant...

The European Union (EU)'s MDR goes into effect on May 2020. This new regulation is complex, presenting a data and design dilemma for Life Science companies, as product labeling will undergo greater scrutiny in the name of patie...

Watch this webinar to understand how to improve your labeling and artwork management processes across your pharmaceutical and medical devices packaging value chain As regulatory scrutiny continues to propagate life sciences, i...

As labeling related regulatory requirements continue to propagate, from Brexit to uDi to MDR, it is vital for Pharmaceutical and Medical Device companies to implement good practice guidelines and technology into their labeling ...

This new EU MDR regulation is complex, presenting a data and design dilemma for Medical Devices companies, as product labeling will undergo greater scrutiny in the name of patient safety. Key Learning Objectives: -Best practic...

The amount of product content Pharma companies continually create and update is simply mind-blowing 🤯 Managing this content data is a monumental task. How do you do this as efficiently, cost-effectively, and accurately as pos...