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Good Laboratory Practice (GLP) Audits & Consultancy

Ensure data integrity. Validate systems. Strengthen pre-clinical compliance.

At IVITAA CONSULTANCY, our GLP services are designed to support both in-house and outsourced non-clinical research environments. We conduct rigorous audits, system validations, and strategic assessments to help organizations maintain compliance with international GLP standards.

Our GLP Support Covers:

DMPK & Toxicology Lab Audits
Comprehensive evaluations of Drug Metabolism and Pharmacokinetics (DMPK) facilities and Non-Clinical/Toxicology departments at sponsor sites and CROs.

Process Mapping & Workflow Optimization
Detailed mapping of laboratory operations to identify process gaps, reduce variability, and enhance compliance efficiency.

DMPK LIMS Validation
Validation oversight of Laboratory Information Management Systems used in DMPK studies to ensure data accuracy, security, and traceability.

LC-MS CDS Validation for Bioanalysis
Verification and validation of Chromatography Data Systems supporting bioanalytical workflows, including LC-MS/MS platforms.

Bioanalytical Method Validation Review
Technical review and critique of bioanalytical method validation reports to assess robustness, reproducibility, and regulatory alignment.

Pre-Clinical Development Consultancy
Advisory support across early-phase research, ensuring scientific rigor and GLP conformity throughout non-clinical study planning and execution.

IVITAA delivers practical, audit-ready solutions to elevate laboratory performance and regulatory confidence in your pre-clinical programs.

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Good Laboratory Practice (GLP) Audits & Consultancy

Ensure data integrity. Validate systems. Strengthen pre-clinical compliance.

Our GLP Support Covers:

DMPK & Toxicology Lab Audits Comprehensive evaluations of Drug Metabolism and Pharmacokinetics (DMPK) facilities and Non-Clinical/Toxicology departments at sponsor sites and CROs.

Process Mapping & Workflow Optimization Detailed mapping of laboratory operations to identify process gaps, reduce variability, and enhance compliance efficiency.

DMPK LIMS Validation Validation oversight of Laboratory Information Management Systems used in DMPK studies to ensure data accuracy, security, and traceability.

LC-MS CDS Validation for Bioanalysis Verification and validation of Chromatography Data Systems supporting bioanalytical workflows, including LC-MS/MS platforms.

Bioanalytical Method Validation Review Technical review and critique of bioanalytical method validation reports to assess robustness, reproducibility, and regulatory alignment.