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.