Agentic OS for LifeSciences

Cut gruntwork. Speed up launches. Stay compliant.
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What Our AI Agents Can Do for Life Sciences

Purpose-built solutions that solve everyday challenges across your teams - fast, accurate, and easy to adopt

Regulatory Affairs

Regulatory teams face growing complexity in coordinating submissions, reviewing dossiers, and responding to agency questions. SyncIQ automates key parts of this process, from reviewing documents to tracking policy changes and generating accurate responses.

Dossier Review

Cross-checks content across modules and templates to flag missing or outdated data.

Labeling Support

Drafts and aligns product labels with market-specific standards and approval history.

Query Resolution

Auto-generates responses to IRs using past data, guidelines, and submission contexts.

Policy Monitoring

Stays informed about FDA, EMA, and PMDA updates with impact assessments.

Manufacturing/QA

QA teams often spend over half their time on reviews, investigations, and documentation. SyncIQ automates EBMR review, deviation analysis, and CAPA preparation by pulling structured data and generating summaries. The result is faster batch release and stronger compliance.

EBMR Review

Validates entries, signatures, and deviations by checking against SOPs and MBRs.

Deviation Analysis

Identifies root causes using templates and past records for consistency and speed.

CAPA Drafting

Recommends corrective actions backed by previous case outcomes and effectiveness data.

Release Support

Compiles traceable summaries for final QA approval and regulatory readiness.

Medical Affairs

MSLs are tasked with preparing briefs, handling complex HCP questions, and entering notes into CRM systems. SyncIQ supports this function by generating compliant answers, creating meeting prep materials, and capturing structured insights automatically.

HCP Briefs

Auto-generates customized pre-call briefs from CRM history, trials, and scientific literature.

Scientific Answers

Responds to on-the-spot HCP questions using trials, publications, and product docs.

CRM Logging

Captures and structures meeting notes and follow-ups directly into the CRM system.

Manage your team with reports

Convert field conversations into structured insights for strategic team review.

Market Access

Market Access teams handle hundreds of dynamic payer, PBM, and government policies. Our AI agents simplify each step by tracking coverage updates, reviewing contracts, and supporting rebate dispute resolution. From formulary checks to post-launch monitoring, SyncIQ removes manual complexity and reduces risk.

Policy Coverage Intelligence

Identifies changes in coverage policies early by scanning payer and government sources.

Contract Review

Draft, compare, and validate rebate agreements with PBMs and payers in structured formats.

Formulary Verification

Confirms drug placement across formularies using integrated, up-to-date source data.

Rebate Dispute Support

Review claims and highlights inconsistencies to reduce lost revenue from chargebacks.

Everything You Need to Automate with Confidence

Our platform is equipped with powerful features that make building, deploying, and managing intelligent agents simple and intuitive.

Domain Expertise

Our platform is co-piloted by functional domain experts from the life sciences industry, ensuring every AI agent and workflow understands your unique challenges.

Domain Data Hub

Proprietary data crawlers for advanced, automated life sciences data acquisition.

Specialized small language models trained for specific life sciences functions.

Connections to data sources like the FDA, PubMed, and formularies.

Integrations Hub

Our platform acts as a central integration hub, connecting with enterprise systems essential to life sciences operations—like Model N, Conga, SharePoint and many more.

Domain-Crafted Agentic Templates & Workflows

Developed by SyncIQ’s in-house life sciences experts for Label Updates, Safety Triage, eCTD Prep

AI Necessity Logic with human-review checkpoints built to GxP & 21 CFR Part 11 standards

Modular, compliance-hardened blueprints you can deploy in days, not months

Agentic Solutions Built for Your Unique Needs

Our multi-agent platform deploys a coordinated digital workforce to master your most critical challenges, enhancing resilience, ensuring compliance, and accelerating speed-to-market.
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Regulatory Co-Pilot Canvas

SyncIQ's Agents accelerate pharma submissions by automating dossier creation, managing agency queries, and ensuring global compliance.
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Formulary Verification Canvas

SyncIQ’s AI agents for formulary verification automate compliance checks, rebate validation, and formulary analysis.
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Frequently asked questions

Everything you need to know about SyncIQ.
What is SyncIQ and how does it differ from traditional AI platforms?
SyncIQ is an agentic-AI platform that coordinates smart AI agents in human-in-the-loop workflows. It comes with built-in domain logic, compliance guardrails, and a visual canvas—unlike standalone models or point-solutions.
What integrations and data sources can SyncIQ connect to (e.g., LIMS, ERP, e-prescribing systems)?
1. ERP (SAP, Oracle)
2. CRM / content stores (Salesforce, SharePoint, Box)
3. Industry platforms (Veeva, Conga)
4. LIMS / MES / e-Prescribing / EHR
5. Regulatory crawlers (FDA, EMA sites)
6. Any REST/SOAP API or database
How do I onboard my team and configure SyncIQ for our specific pharma or life-sciences processes?
We guide you end-to-end: a discovery call, sandbox POC, tailor prebuilt agents to your workflows, then phased rollout and optimization—backed by our expert services.
What security, privacy, and data governance standards does SyncIQ adhere to?
Enterprise-grade by design: TLS 1.2+ in transit; AES-256 at rest; role-based access; SSO/SAML; SOC 2 Type II; GDPR/HIPAA-ready; VPC or on-prem options.

Get Started in Just a Few clicks

Contact us to schedule your demo today.