Resources at TruoX Laboratories
Technical materials, regulatory insights, and client tools to support your quality journey.
What You’ll Find Here
As TruoX builds out its GMP infrastructure, this page will become home to resources designed to support pharmaceutical developers, sponsors, and biotech teams. Content will include:
- Sample submission forms and intake checklists
- Regulatory timelines and ICH guidelines summaries
- Template documents (CoAs, method validation outlines)
- Investor materials (pitch deck, roadmap)
- Industry whitepapers and GMP explainers
If you're looking for something specific, feel free to contact us directly.
Need a specific resource?
Reach out and we’ll get you what you need — whether it’s a sample CoA, reference document, or onboarding file.
Request a Document