ABOUT US

Resero Analytics

Founded in 2018 and headquartered in Indianapolis, Indiana.

 

Our vision is to build modern, scalable digital platforms that are the backbone of leading drug development organizations so that large pharma, biotechs, and CROs discover drugs more quickly and with greater confidence.

 

Resero Analytics software reduces the friction of legacy LIMS systems for study execution, analysis, and regulatory reporting. Our TurboPlatform unifies study design, laboratory operations, scientific interpretation, and compliance in a single validated environment built for modern drug development.

 

TurboPlatform helps toxicologists, pathologists, PK scientists, and bioanalytical teams:

  • Run study execution, laboratory operations, and reporting in one scalable platform
  • Move from protocol to regulatory submission faster and with greater confidence
  • Ensure full compliance with GLP, SEND standards, ICH guidance, and eCTD expectations
By combining automation with rigorous data architecture, Resero turns complex
experimental data into regulatory-ready submissions efficiently and reliably.

Meet the Leadership Team

David Watson, Ph.D.

Chief Executive Officer

  • Built and commercialized deterministic scientific software for regulated environments.
  • 20 years of large pharma experience across toxicology, PK/TK, and regulatory engagement with FDA and EMA.
  • Founder-led enterprise sales and strategic partnerships with large pharma and CROs.

Anil Gunturu

Chief Technology Officer

  • Architected the modern, scalable TurboPlatform stack replacing legacy LIMS infrastructure.
  • Senior engineering team delivering production systems in under six-month cycles across LIMS, PK/TK, and toxicology.
  • Product leadership integrating discovery and regulatory workflows with governed AI.

C. Edwin Garner

VP of Modeling & Simulation

  • 30 years of experience in translational pharmacology,
    modeling, and simulation supporting drug development programs
  • Deep expertise in IVIVE, mechanistic modeling, and quantitative interpretation of PK and pharmacology data
  • Advisor to biotechnology companies on translational strategy, integrating preclinical findings to support human dose prediction and development decisions

Taylor Scott

Product Manager

  • 6 years at Resero, leading customer engagement and product definition for AI-powered scientific software in the pharmaceutical industry

  • Bridges scientific user needs and software capabilities through specifications and workflow design
  • Drives adoption of high-quality solutions through product
    demonstrations, coordinated deployments, and iterative product refinement

David Watson, Ph.D.

Founder & CEO

Resero Analytics is building the software Dave wished he had in Pharma where he helped develop small molecules, peptides, and antibodies for infectious diseases, diabetes, and oncology.

Anil Gunturu

CTO

Responsible for guiding technology strategy and system architecture for Resero’s innovative products, while also contributing to the overall vision and long-term strategy.

C. Edwin Garner, Ph.D.

VP of Modeling & Simulation

C. Edwin Garner, Ph.D. has 25 years of experience in the drug discovery and development arena from startups to large pharma (DuPont/Merck, Schering-Plough, AstraZeneca). He is responsible for guiding scientific strategy and implementation of Resero’s innovative modeling products and services. He is an expert in classical pharmacokinetic and PBPK modeling/simulation based translation of preclinical PK and PD to the clinical environment.

Andrew Vick, Ph.D.

Advisor

Responsible for corporate development, leveraging 28 years of experience in biotech and in the pharmaceutical industry across both innovator and supplier roles. His expertise spans toxicology, nonclinical and clinical pharmacology, and drug disposition, helping drive growth and strategic partnerships.

Taylor Scott

Product Manager

Responsible for client relationships by demonstrating our products, coordinating efficient deployments, and refining product designs to meet client needs.

Chris Campetti

Software Engineer

Responsible for frontend technologies, like React, and collaborating with the backend team to assure our technology stack is performant and accurate to the functional design.

Sunny Arora

Senior Backend and DevOps Engineer

Responsible for designing and optimizing scalable backend system, automating workflows, and managing infrastructure to ensure system reliability and delivery of efficient solutions through robust CI/CD practices.

Angelo Dalde

QA Tester

Responsible for designing the manual test suite for software releases to ensure compliance with the requirement specifications and high quality standards.

Satvik Sharma

Software Engineer

Responsible for designing and coding the TurboProposal user interface, ensuring a seamless and intuitive user experience.

Andy Dahlem

Business Advisor

Andy served as VP of R&D at Eli Lilly, with numerous responsibilities including for Toxicology and Drug Disposition, R&D Strategy, Due Diligence, and Competitive Intelligence. He also served as Chief, Division of Clinical Pharmacology, at the Indiana University School of Medicine.

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