October 22, 2020

Oncopeptides implements Veeva QualityDocs in 6 weeks

Past event

About the event

Epista provides Veeva advisory and implementation services to help Oncopeptides get to market faster with lower risk.

Time and place

October 22, 2020
3:00 pm
4:00 pm

Why you should join

Get the webinar

Oncopeptides is committed to the development of therapies for difficult-to-treat hematological diseases. They’re one of Epista’s clients driving innovations that improve health care around the world. Oncopeptides is quickly transforming from a small R&D outfit to a full-blown pharmaceutical production company. Epista's Veeva Certified Partner team helped them select, implement (in only 6 weeks), and now, operate their Veeva QualityDocs system, so they can get to market fast while establishing processes for the long term.

Implementing a new document management system can be challenging, raising technical issues, and creating new risks. Further, when you consider the scope of a full Veeva project – migration, integration, validation, and more, it can appear even more daunting. But it doesn’t have to be that way. Watch this webinar to learn how Epista’s experts brought their in-depth understanding of business, compliance, and IT systems and the required technical abilities to support Oncopeptides as a Veeva advisory and implementation partner.

You’ll hear from Catarina Lundhagen Stensils, QA & Process Coordinator at Oncopeptides, and Karin Hesslevik, Compliance Consultant at Epista Life Science. Catarina and Karin discuss:

  • Translating Oncopeptides’ business priorities into the right system decision
  • How Epista’s team provided Veeva advisory support
  • How Oncopeptides efficiently implemented Veeva QualityDocs under significant time and resource constraints
  • What changes were required after go-live
  • How Oncopeptides will handle ongoing operations to keep them prepared for the future

Keynote Speakers

Karin Hesslevik

Principal Consultant

Catarina Lundhagen Stensils

Quality Assurance Manager

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