A consortium of law firms leading a national pharmaceutical multidistrict litigation (MDL) required large-scale medical record review support for more than 12,000 plaintiffs. Over 12,000 plaintiffs were involved in the action and the legal team required an experienced partner that could handle medical records under tight court deadlines while ensuring accuracy and consistency in every case.
The law firm consortium faced the demanding task of processing medical records for more than 12,000 plaintiffs, all within a strict 90-day timeframe. Before the upcoming bellwether trials, each plaintiff's case required extensive medical records to be reviewed, organized and converted into accurate medical chronologies.
The project became increasingly difficult because of several factors:
To support one of the country's largest pharmaceutical MDL projects, LezDo TechMed implemented a structured medical record review process designed to handle thousands of plaintiff cases within the required project timeline. By combining experienced reviewers with standardized workflows and organized project oversight, consistent medical record reviews were delivered across the entire plaintiff population.
LezDo TechMed assigned a team of 50 skilled medical reviewers to the project. The team was able to review thousands of plaintiff records simultaneously while maintaining consistent turnaround times and review quality throughout the project by allocating specialized resources to the engagement.
To maintain consistency across all plaintiff cases, standardized medical chronology templates were created before the review process began. Every medical chronology was prepared using a consistent structure, giving attorneys a straightforward way to review and compare case information. This made the chronologies easier for attorneys to analyze and compare during case evaluations, bellwether trial preparation and settlement planning.
To capture the medical information most relevant to the litigation, a customized data extraction protocol was implemented. Key clinical events, diagnoses, treatment history, medications and other case-specific details were consistently identified and reviewed by the reviewers. The process produced clear and standardized medical chronologies, making it easier to examine medical evidence across thousands of cases.
A centralized platform brought all project information together, allowing the team to monitor case progress, quality reviews, and completed chronologies from a single location. While maintaining project information, this structured approach enhanced collaboration across review teams.
Project managers used real-time analytics dashboards to monitor daily progress, spot workflow bottlenecks and redistribute reviewer workloads as project demands changed. Ongoing oversight of daily activities helped sustain a balanced workflow and supported timely completion of project milestones.
To manage the large volume of plaintiff records efficiently, LezDo TechMed implemented a systematic review process that guided each stage of the engagement, from record intake through the delivery of completed medical chronologies. Every stage was carefully coordinated to ensure consistency, transparency and timely completion across all plaintiff cases.
The execution process included:
Intake — Plaintiff medical records were received from the consortium and logged into the centralized system.
Organization — Before the review stage, medical records were systematically arranged and categorized for each plaintiff to streamline case processing.
Review & Extraction — After reviewing each plaintiff's medical records, the team compiled the relevant clinical history into a structured chronology that supported legal case assessment.
Chronology Creation — Extracted data was compiled into a standardized medical chronology for each plaintiff.
Quality Review — Every chronology passed through a quality check to confirm accuracy and consistency before release.
Submission — Approved medical chronologies were delivered through the centralized project platform, providing the legal team with timely access for ongoing case preparation.
LezDo TechMed enabled the law firm consortium to manage one of the largest pharmaceutical MDL documentation projects within the required litigation timeline by implementing a structured medical record review process. The project was completed with high accuracy, consistent quality, and seamless coordination across thousands of plaintiff cases.
Key Outcomes:
Working with the team gave us confidence that every case was handled with care and consistency. Their ability to manage a large volume of medical records without affecting quality was invaluable to our litigation preparation.
— U.S.-Based Product Liability Law Firm
This project demonstrated that a well-planned medical record review strategy can effectively support large-scale pharmaceutical MDL litigation while maintaining accuracy, consistency and strict deadline compliance. By delivering consistent medical chronologies within demanding timelines, LezDo TechMed helped the law firm consortium maintain momentum throughout critical stages of case preparation.
Preparing for your next MDL or mass tort litigation? Find out how LezDo TechMed delivers litigation-ready medical record review services tailored to large-scale legal projects.
Jerin Jose Nesamony is the Founder and CEO of LezDo TechMed, a medical data analysis company he established in 2013 with a background in healthcare operations and multispecialty hospital settings. Skilled in bridging complex medical documentation with legal and insurance workflows, he understands the precision and compliance demands that drive high-stakes medico-legal decisions. He leads the development of technology-driven solutions — including the proprietary CaseDrive platform — that help law firms, insurers, IMEs, QMEs, and life care planners across the U.S. streamline medical record review, improve case outcomes, and operate with greater efficiency.