An end-to-end biostatistics automation platform.
To deliver faster, more efficient, high-quality clinical trial results.
idaptiq automates and connects the core biostatistics deliverables required for FDA and other regulatory submissions — SAP, SDTM, ADaM, and TLFs — reducing labor and accelerating clinical trial timelines.
Our Platform
Core Documents
Protocol, CRFs, Database Specifications.
SAP
Text + TLF Shells.
SDTM
Specifications + Code + aCRF.
ADaM
Specifications + Code + TLF shell annotations.
TLF
TLF Code.
idaptlinq™
Links biostats deliverables, automating downstream re-work when protocol amendments or other changes are identified with automatic dependency detection.
Meeting customer needs.
We partner directly with our biopharma and CRO customers to transform how they are completing their biostatistics activities.
Human expertise remains central
The platform augments biostatisticians and programmers rather than replacing them. Human review, judgment, and accountability remain essential throughout the workflow.
Secure and compliant system by design
Platform security and privacy are held at the study level, customer level, and system level. Every study is in an isolated and secure tenant. All information is encrypted at rest and in transit. The system meets GxP and Part 11 compliance requirements.
Patient data protection is absolute
Patient data is not processed or stored in the idaptiq cloud and does not go through an LLM.