4 min read
What is a Scientific & Medical Publications Professional?
Would your drug development program benefit from partnering with experts in scientific and medical communications and...
As you look to transition your compound into clinical trials, you need the right partner to guide your planning and decision-making. Whether you are preparing your IND/CTA, or you are looking to recruit patients quickly to get your early phase trials running, or just need medical writing or biostatistical support for your programs – Veristat can help.
We provide impactful solutions on both a full-service or functional service basis, including strategic regulatory guidance, clinical program design, and IND/CTA support through to successful regulatory approval.
Veristat team member Philip Ho , Business Development Director, Asia Pacific, will be at the venue— ready to listen to your needs and share Veristat’s expertise
Schedule a meeting by filling out the form on the right. Find out how we can help you advance your next clinical trial or regulatory submission to successful outcomes.

Website: Bio Asia Taiwan
4 min read
Jun 23, 2026 Veristat Blog
Would your drug development program benefit from partnering with experts in scientific and medical communications and...
7 min read
Jun 19, 2026 Rachel Abu Taleb
A look at where personalized mRNA cancer vaccines, in vivo CAR-T and TIL therapies stand after this year’s meeting
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