4 min read
ASCO 2026: RAS Is No Longer Undruggable
For decades, oncologists and drug developers shared an undeniable truth: KRAS – one of the most commonly mutated genes...
Advancing Gene Therapies for Patients with Rare Diseases and Limited Treatment Options.
Veristat is proud to participate in the 8th Annual Gene Therapy Development Summit, a premier event being held in Boston, MA, March 25-27, dedicated to transforming the future of gene therapies for rare and common diseases.
Your Gene Therapy Development Partner
At Veristat, we specialize in bringing revolutionary therapies to life. The knowledge we have amassed over 30 years has been game-changing for sponsors. From strategic planning and clinical trial execution to regulatory consulting, our creative approaches have helped them overcome daunting evidentiary and regulatory hurdles to gain swift and successful therapy approval. Tailored Strategies and Expert Insights
With 35% of our work supporting rare and ultra-rare diseases, Veristat brings unmatched experience to gene therapy programs. In the past five years, we’ve:
We ensure rare disease trials qualify for accelerated regulatory pathways, such as Orphan Drug Designation or Priority Review, and support your team through every milestone to bring therapies to patients faster.
Meet with Veristat:
Erin Gaffney - Senior Business Development Director
Schedule a meeting with Erin to discuss how Veristat can accelerate your gene therapy program.
Learn more about the conference
4 min read
Jun 15, 2026 Veristat News
For decades, oncologists and drug developers shared an undeniable truth: KRAS – one of the most commonly mutated genes...
10 min read
Jun 12, 2026 Veristat Blog
This May 2026 regulatory update highlights multiple guidances issued by the FDA across cell and gene therapy, clinical...