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Pharma Launches Don’t Fail Because of Strategy. They Fail Because of Documents.

Discover how Veeva + Adlib eliminate content bottlenecks, accelerate approvals, and make your launches AI-ready.

Why Read This Ebook?

Bringing a drug to market is a pressure cooker:

  • Tight timelines and a 20-year patent clock
  • 10,000+ documents that all need to be compliant and submission-ready
  • $1M lost revenue every day a launch is delayed

Veeva Vault is the industry backbone for regulated content. But here’s the truth:

  • Veeva wasn’t built to clean up messy PDFs, validate regulatory bundles, or prevent document rejection.
  • That’s where Adlib comes in.

 

What You’ll Learn Inside

  • The hidden cost of bad content – why broken formats, missing metadata, and rekeying errors drain millions.
  • How Adlib accelerates Veeva – turning scanned files, CAD drawings, and clinical reports into validated, AI-ready assets.
  • Real-world numbers – thousands of docs per month, 30% rejection rates, and $1,000 per fix… and how Adlib automates that risk away.
  • The AI advantage – why Veeva + Adlib is the launch stack that makes AI accurate, audit-safe, and scalable.

 

Who Should Read It?

  • Regulatory Affairs Leaders preparing submission packages
  • Clinical Operations Teams buried in site docs and SOPs
  • Quality Executives chasing audit readiness
  • Pharma Executives focused on launch speed and compliance ROI

 

Don’t let documents derail your launch.
Download the ebook and see how Veeva + Adlib make compliance, speed, and AI success possible from Day One.