When your product is linked to an injury, every decision depends on what the medical records actually say. From managing mass tort MDL proceedings to addressing individual product liability claims, LezDo TechMed transforms complex medical documentation into evidence you can count on — and evidence that holds up.
Powered by CaseDrive, our AI-assisted case review platform, we streamline medical record analysis at scale — helping manufacturers, defense counsel, and risk management teams uncover the facts, challenge weak claims, detect pre-existing conditions, and build defensible, litigation-ready strategies.
Product liability and mass tort cases are among the most documentation-intensive legal proceedings a manufacturer will face.
The core challenge is not just volume, it is precision. A misread timeline or inconsistent analysis across plaintiffs can undermine an entire defense strategy.
LezDo TechMed provides product manufacturers, defense counsel, and risk management teams with the clinical intelligence they need at every stage of proceedings.
We provide end-to-end medical record analysis structured around the specific evidentiary demands of product liability and mass tort defense, from initial claim assessment to courtroom-ready documentation.

Our clinical team builds precise causation timelines from medical records, giving your experts and counsel the evidentiary foundation, they need.
We apply standardized review frameworks across all plaintiffs — maintaining uniform analysis regardless of volume or jurisdiction.

Every report is formatted to meet legal, regulatory, and audit requirements, without your team having to reformat or reprocess

Our cross-case pattern analysis helps manufacturers identify systemic safety concerns early, before the next claim arises.
We partner with product manufacturers to simplify complex medical record analysis — making it consistent, defensible, and litigation-ready at every stage of the claim process.
Evidence you can rely on in litigation or internal reviews.
Accelerated timelines without sacrificing quality and accuracy.
HIPAA-compliant processes with encryption and secure data handling.
Scale up to high-volume mass tort litigation.
Standardized reports ensure findings hold up under legal and regulatory scrutiny.
CaseDrive's centralized dashboard gives all your teams a real-time view of every case.
Trusted by leading manufacturers facing high-stake mass torts/MDLs.
Experience our process with a free pilot review to see how we can strengthen your legal strategy.
Stronger case strategies
Faster case preparation
Faster Defense
Fewer Weak Claims
Stronger Evidence
Reduced liability
From Records to Defense-Ready Intelligence
Medical records submitted via— HIPAA-compliant CaseDrive, accessible to all authorized team members in real time.
AI extracts, classifies, and structures medical data from clinical notes, imaging, operative reports, and device documentation

Board-certified medical professionals audit every AI output for clinical accuracy, causation assessment, and legal defensibility.

For mass tort cases, data is cross-referenced across plaintiff pools to identify injury patterns, failure modes, and outliers.

Litigation-ready reports delivered within 48 hours — with full source citations, audit trails, and real-time CaseDrive tracking.
See how we handle causation analysis, pre-existing condition documentation, alternative cause identification, and defense-ready report formatting for your case.
Got common questions on our product liability medical record review? Check here!
Medical record review for product manufacturers is a specialized clinical analysis service that examines claimant medical records in product liability and mass tort cases. It involves causation analysis, pre-existing condition identification, injury pattern analysis across plaintiff groups, and the creation of litigation-ready chronologies and summaries that support product defense strategy. LezDo TechMed delivers this service with a 99.8% accuracy rate and a 48-hour standard turnaround.
In mass tort MDL proceedings, medical record review provides three critical functions: standardized causation analysis across all plaintiffs, cross-plaintiff injury pattern detection to identify failure modes and complication clusters, and bellwether case preparation support. LezDo TechMed applies uniform review frameworks across entire plaintiff pools — ensuring consistent findings regardless of MDL volume or jurisdiction.
We conduct systematic assessment of each claimant's full medical history — identifying comorbidities, prior injuries, lifestyle factors, and non-product-related medical events. Our alternative cause analysis documents pre-existing conditions with clinical precision, distinguishing them from alleged product-related harm. This analysis is sourced directly from the medical record and is fully defensible in litigation.
Causation analysis is the clinical process of determining whether a specific product, exposure, or event caused a claimant's reported injury. LezDo TechMed builds detailed causation timelines that link product use or implantation to symptom onset, diagnostic findings, and clinical progression — documenting temporal relationships between product exposure and injury. This forms the evidentiary foundation for both defense arguments and expert witness testimony.
Yes. We specialize in medical device litigation, creating chronologies that capture device implantation dates, device specifications (model, lot number, size), surgical details, complication onset, imaging findings, and revision or removal procedures. Our reviewers understand FDA device classifications, recall histories, and failure mechanisms — bringing regulatory context that general medical reviewers cannot.
Yes. We systematically extract and document device identifiers — lot numbers, serial numbers, manufacturing dates, model variations, and device specifications — from operative reports, device cards, and medical records. This cross-plaintiff tracking is critical for identifying defective product batches and supporting manufacturing defect arguments in MDL proceedings.
We support all major product liability categories: medical devices and implants (joint replacements, surgical mesh, IVC filters, spinal implants, cardiovascular devices), pharmaceutical products (drug-induced injuries, prescription and OTC medication complications), consumer products, automotive defects, and industrial equipment failures. Our team has analyzed over 8,500 product liability cases across 200+ product types.
Our standard turnaround is 48 hours for individual cases. For high-volume MDL proceedings, we deploy dedicated review teams to maintain the same 48-hour standard at scale. All deliverables are tracked in real time through CaseDrive, our HIPAA-compliant case management platform.
Yes. All records are processed through CaseDrive, our HIPAA-compliant, SOC 2 Type II certified platform with end-to-end encryption. We are also ISO 9001 and ISO 27001 certified. Our processes meet the data security requirements of the most rigorous legal, regulatory, and corporate environments.
Yes. We offer a free pilot review — one complete case processed by our full clinical team, delivered through CaseDrive at the standard 48-hour turnaround — before any commitment. This allows you to evaluate our causation analysis quality, report format, and platform workflow on a real case from your portfolio.
From individual claims to large-scale MDL proceedings — LezDo TechMed delivers the clinical intelligence your defense demands.