Webinars image Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them
Artwork
<1 min read
by Schlafender Hase

Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them

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RAPS webinar: e-Labeling and what it means for regulatory teams
Webinars
RAPS Webinar
2 min read
by Schlafender Hase
RAPS webinar: e-Labeling and what it means for regulatory teams

Regulatory Affairs (RA) professionals play a critical role in safeguarding product integrity and compliance during the packaging artwork process. Yet despite rigorous review cycles, errors still slip through, from incorrect claims and dosage instructions to misaligned barcodes or outdated reference text. These mistakes not only delay approvals but can lead to costly recalls and reputational damage.

In this webinar, we break down the most common pitfalls RA teams face when reviewing artwork, how to mitigate the risk of errors and ensure compliance with regulatory standards throughout the process

We’ll also demonstrate how TVT, the automated proofreading solution for regulated industries, helps RA professionals:

  • Detect deviations instantly, no matter the file type, layout, or language.
  • Eliminate manual, error-prone checks.
  • Provide a fully validated, audit-ready process that satisfies regulatory requirements.

Learning outcomes:

  • Understanding top pitfalls RA teams encounter in document review and why they persist
  • Proven strategies to build an efficient review process
  • How automated proofreading and artwork checks with TVT reduces risk of errors going to market, speed up approvals, and ensure audit-ready compliance

Presenters:

Katarina Kresankova

Katarina got her Master´s Degree in Translating and Interpreting. After spending a few months as a trainee in the European Parliament translation unit, she found her passion in sales where she has been working for over 10 years with a focus on the IT industry. Since 2020, she has been a part of the sales team at Schlafender Hase, where she can combine her knowledge in sales with understanding of the importance of text accuracy backed up by her academic background.

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Dean Halliday

Dean Halliday has been working with customers in highly regulated markets for over a decade and specialises in working with the Life Science Industry. Ensuring that the related risks of manual proofreading and approval processes are identified and solved quickly and easily, allowing only approved content to be printed or published.

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