SmartX Protocol generates analytical method development protocols, dev reports, and validation documents in minutes — not days.
Analysts spend days drafting method development protocols from scratch, repeating the same structure across molecules.
Reusing old reports introduces stale data, wrong molecule names, and inconsistent parameters that slip through review.
Every analyst formats differently. Templates drift over time. Audits flag the inconsistencies, and QA spends hours fixing them.
Generate complete method development protocols for HPLC and dissolution testing with drug-specific parameters auto-filled.
Structured dev reports with method rationale, column screening results, and optimized conditions — ready for review.
ICH-compliant validation protocols and reports covering specificity, linearity, accuracy, precision, and robustness.
Templates aligned with USP, EP, and BP pharmacopeial standards. Consistent formatting across every document, every time.
Regulated industry experience. We've built compliant systems for finance, healthcare, energy, and public sector — industries where accuracy isn't optional.
Enterprise-grade integrations. Secure API architectures with mTLS, REST, and data exchange across complex systems — not duct-taped scripts.
Purpose-built AI. Not a ChatGPT wrapper. Our AI is trained on pharma analytical workflows — it understands your domain, your terminology, your standards.
Web & mobile ready. Modern platform accessible from any device. Built for how QA teams actually work — in labs, at desks, and on the go.
Watch how a complete HPLC method development protocol gets generated in under 2 minutes.
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