Industry Solutions

Built for Your Industry

Every laboratory is unique. LabZila adapts to your industry's specific workflows, compliance requirements, and operational challenges with purpose-built configurations.

Pharmaceutical & Biotech

Accelerate Drug Development with GMP-Ready LIMS

Pharmaceutical and biotech laboratories operate under the most stringent regulatory demands in any industry. From raw material testing through final product release, every data point must be traceable, every process validated, and every record audit-ready. LabZila provides a purpose-built platform that embeds compliance into your daily workflows rather than layering it on as an afterthought.

Key Industry Challenges

Maintaining 21 CFR Part 11 compliance across all electronic records
Managing complex stability study protocols over extended timelines
Ensuring data integrity during method validation and transfer
Tracking batches across multi-site manufacturing operations

How LabZila Helps

  • 21 CFR Part 11 Electronic Signatures — Secure e-signatures with full audit trails, password re-authentication, and signature meaning capture
  • Stability Study Management — Automated pull scheduling, condition monitoring, and ICH-compliant trend analysis with configurable protocols
  • Method Validation Workflows — Structured protocols for accuracy, precision, linearity, range, and robustness with auto-calculated acceptance criteria
  • Batch Record Integration — Link analytical results directly to batch records with full genealogy and deviation tracking
  • OOS/OOT Investigation — Guided out-of-specification and out-of-trend investigation workflows with root cause analysis and CAPA integration

Compliance Standards Supported

21 CFR Part 11

FDA electronic records and electronic signatures regulation for pharmaceutical manufacturing

EU Annex 11

European guidance on computerised systems used in GMP-regulated environments

cGMP / GLP

Current Good Manufacturing Practice and Good Laboratory Practice standards

ICH Guidelines

International Council for Harmonisation stability testing, validation, and quality guidelines

USP / EP / JP

Pharmacopeia method references and monograph compliance for testing standards

Compliance Standards Supported

CLIA

Clinical Laboratory Improvement Amendments for quality standards in laboratory testing

CAP Accreditation

College of American Pathologists accreditation checklist compliance and inspection readiness

ISO 15189

International standard specifying requirements for quality and competence in medical laboratories

HIPAA

Health Insurance Portability and Accountability Act for patient data privacy and security

HL7 / FHIR

Healthcare interoperability standards for seamless integration with EHR and HIS systems

Clinical Diagnostics

Deliver Faster, More Accurate Patient Results

Clinical laboratories face relentless pressure to reduce turnaround times while maintaining diagnostic accuracy. With growing test volumes and expanding test menus, manual processes create bottlenecks that delay critical patient care decisions. LabZila streamlines every step from sample accessioning to result delivery, helping your lab meet the demands of modern healthcare.

Key Industry Challenges

Reducing turnaround time for critical and stat specimens
Maintaining accurate patient sample chain of custody
Preparing for CAP and CLIA inspections with complete documentation
Integrating results with hospital EHR and physician ordering systems

How LabZila Helps

  • Patient Sample Tracking — Barcode-driven accessioning with positive patient ID verification and automated aliquot management
  • Turnaround Time Monitoring — Real-time TAT dashboards with automatic escalation alerts when specimens approach SLA thresholds
  • Accreditation Support — Pre-built CAP checklist mappings, proficiency testing management, and inspection-ready reporting
  • Automated Result Reporting — Rules-based auto-verification with reflex and add-on test logic, critical value notification, and delta checks
  • QC & Westgard Rules — Built-in Levey-Jennings charts with multi-rule QC violation detection and automatic lockout capabilities
Environmental Testing

Protect Communities with Reliable Environmental Data

Environmental laboratories must deliver defensible data that stands up to regulatory scrutiny and legal challenge. From drinking water compliance monitoring to contaminated site assessments, the accuracy of your results directly impacts public health and environmental protection. LabZila provides the robust chain of custody, method management, and reporting capabilities that environmental testing demands.

Key Industry Challenges

Maintaining defensible chain of custody from field to final report
Meeting strict hold times and preservation requirements for diverse matrices
Generating state- and EPA-specific electronic data deliverables
Managing high sample volumes with complex multi-analyte test panels

How LabZila Helps

  • Chain of Custody Management — Digital COC with tamper-evident tracking from field collection through sample receipt, storage, and disposal
  • Hold Time Monitoring — Automated alerts for approaching and expired hold times with preservation requirement verification at login
  • EPA EDD Generation — One-click generation of EQUIS, STORET, WQX, and state-specific electronic data deliverable formats
  • Field Sampling Integration — Mobile-friendly sample collection with GPS coordinates, field measurements, and photo documentation
  • Multi-Matrix Support — Pre-configured workflows for water, wastewater, soil, sediment, air, and waste matrices with method-specific QC requirements

Compliance Standards Supported

EPA Methods

Full support for EPA 500, 600, and 8000 series methods including method-specific QC requirements

ISO 17025

General requirements for the competence of testing and calibration laboratories

SDWA / CWA

Safe Drinking Water Act and Clean Water Act compliance monitoring and reporting

NELAP / TNI

National Environmental Laboratory Accreditation Program and The NELAC Institute standards

RCRA / CERCLA

Hazardous waste characterization and Superfund site assessment reporting requirements

Compliance Standards Supported

FSMA

FDA Food Safety Modernization Act preventive controls and supply chain requirements

HACCP

Hazard Analysis and Critical Control Points systematic food safety management

ISO 22000 / FSSC 22000

International food safety management system standards and certification scheme

SQF / BRC / IFS

GFSI-benchmarked food safety certification standards for global supply chains

FDA 21 CFR 117

Current Good Manufacturing Practice, hazard analysis, and risk-based preventive controls for human food

Food & Beverage

Safeguard Product Quality from Farm to Table

Food and beverage laboratories are the last line of defense between consumers and unsafe products. Whether you are testing raw ingredients, monitoring production environments, or validating finished goods, your lab must deliver fast, accurate results to keep production lines moving without compromising safety. LabZila helps food labs balance speed with rigor across every testing scenario.

Key Industry Challenges

Rapid pathogen detection to prevent contaminated product release
Managing environmental monitoring programs across production facilities
Tracking shelf life studies and accelerated aging protocols
Meeting multi-framework audit requirements across global markets

How LabZila Helps

  • Microbiological Testing Workflows — Dedicated workflows for pathogen screening, indicator organisms, and sterility testing with incubation tracking and reading schedules
  • Environmental Monitoring — Facility zone mapping, swab site management, scheduled sampling plans, and trend analysis for Listeria and other organisms
  • Shelf Life Management — Configurable study protocols with automated pull scheduling, sensory evaluation tracking, and statistical shelf life prediction
  • Nutritional Label Verification — Proximate analysis tracking with FDA-compliant rounding rules and nutrition facts panel data export
  • Supplier Qualification — Incoming material inspection workflows with supplier scorecards, COA verification, and risk-based sampling plans
Cannabis Testing

Navigate Complex Cannabis Regulations with Confidence

Cannabis testing laboratories operate in one of the most rapidly evolving regulatory landscapes in the industry. With requirements varying by state, changing frequently, and covering everything from potency profiling to contaminant screening, labs need a system that can adapt as fast as the regulations do. LabZila provides cannabis-specific workflows that keep your lab compliant while maximizing throughput.

Key Industry Challenges

Keeping pace with frequently changing state-specific testing requirements
Generating compliant Certificates of Analysis for each jurisdiction
Integrating with state seed-to-sale traceability platforms
Scaling operations rapidly as new markets open and volumes grow

How LabZila Helps

  • Potency Testing Workflows — Cannabinoid profiling with THC/CBD quantification, total potency calculations, and dry-weight conversion per state formulas
  • Contaminant Screening — Integrated panels for pesticides, heavy metals, residual solvents, mycotoxins, and microbial contaminants with state-specific action levels
  • State Compliance Engine — Configurable rule sets for each state's testing requirements, action levels, and reporting formats with automatic updates
  • COA Generation — Professional, state-compliant Certificates of Analysis with QR code verification, batch details, and complete analytical results
  • Seed-to-Sale Integration — Direct API connections to Metrc, BioTrack, and other state traceability systems for automated manifest and transfer reporting

Compliance Standards Supported

State Regulatory Frameworks

Configurable compliance for all active state cannabis testing regulations including CA, CO, OR, MI, and more

ISO 17025

Laboratory accreditation standard increasingly required by state regulators for cannabis testing labs

Metrc / BioTrack

Direct integration with state-mandated seed-to-sale traceability platforms for automated reporting

AOAC Methods

Association of Official Analytical Chemists validated methods for cannabis potency and contaminant testing

2018 Farm Bill (Hemp)

Federal hemp testing requirements including total THC calculation and USDA sampling protocols

Don't See Your Industry?

LabZila is built to adapt. Our configurable platform supports any laboratory type with custom workflows, compliance frameworks, and reporting formats. Talk to our team about your specific requirements.