DIA Global Annual Meeting 2026

Philadelphia, PA

Philadelphia, PA

June 14-18, 2026 | Pennsylvania Convention Center | Philadelphia, PA

Peer AI is exhibiting at the DIA 2026 Global Annual Meeting, the largest multidisciplinary gathering in life sciences. The week brings together industry, regulators, academics, and patient advocates from over 50 countries for conversations on drug development, regulatory strategy, and the technologies shaping how new therapies get to patients.

Visit Peer AI at Booth 1912

Meet the team and see live demonstrations of the platform that biotechs and top 20 pharmas trust to author, orchestrate, and anticipate across the regulatory submission lifecycle. The team will walk through how Peer AI drafts CSRs, protocols, module summaries and more; giving leaders real-time visibility into where every document stands, and helps teams anticipate regulatory questions before they file.

Live Session: "What Survives Inspection: The Data Infrastructure That Makes AI Submission-Grade"
Tuesday, June 16 · 01:05 PM · Innovation Theater 2

Creating regulatory-grade submission documents using AI is more than just content generation. It requires purpose-built data infrastructure – pre-committed source bindings, replayable runs, production corrections that become training signals, and a domain-specific agent harness built for regulated workflows. Anita Modi, Co-Founder and CEO of Peer AI, walks through the architectural design that separates a writing tool from a submission platform, with case studies from real production deployments at biotech and Top 20 pharma customers. Attendees will leave with a framework for evaluating AI solutions built for sustained regulatory scrutiny.

Event details
  • Dates: June 14-18, 2026

  • Location: Pennsylvania Convention Center, 1101 Arch Street, Philadelphia, PA 19107

  • Booth number: 1912

June 14-18, 2026 | Pennsylvania Convention Center | Philadelphia, PA

Peer AI is exhibiting at the DIA 2026 Global Annual Meeting, the largest multidisciplinary gathering in life sciences. The week brings together industry, regulators, academics, and patient advocates from over 50 countries for conversations on drug development, regulatory strategy, and the technologies shaping how new therapies get to patients.

Visit Peer AI at Booth 1912

Meet the team and see live demonstrations of the platform that biotechs and top 20 pharmas trust to author, orchestrate, and anticipate across the regulatory submission lifecycle. The team will walk through how Peer AI drafts CSRs, protocols, module summaries and more; giving leaders real-time visibility into where every document stands, and helps teams anticipate regulatory questions before they file.

Live Session: "What Survives Inspection: The Data Infrastructure That Makes AI Submission-Grade"
Tuesday, June 16 · 01:05 PM · Innovation Theater 2

Creating regulatory-grade submission documents using AI is more than just content generation. It requires purpose-built data infrastructure – pre-committed source bindings, replayable runs, production corrections that become training signals, and a domain-specific agent harness built for regulated workflows. Anita Modi, Co-Founder and CEO of Peer AI, walks through the architectural design that separates a writing tool from a submission platform, with case studies from real production deployments at biotech and Top 20 pharma customers. Attendees will leave with a framework for evaluating AI solutions built for sustained regulatory scrutiny.

Event details
  • Dates: June 14-18, 2026

  • Location: Pennsylvania Convention Center, 1101 Arch Street, Philadelphia, PA 19107

  • Booth number: 1912

Ready to accelerate document creation?

See why biotechs and pharmas trust Peer AI to deliver high-quality, inspection-ready documents.

Cta Image

Ready to accelerate document creation?

See why biotechs and pharmas trust Peer AI to deliver high-quality, inspection-ready documents.

Cta Image

Ready to accelerate document creation?

See why biotechs and pharmas trust Peer AI to deliver high-quality, inspection-ready documents.

Cta Image