Quality Assurance

  • A designated Quality Assurance Programme exists at Intox, following the OECD Guidance document.
  • Our independent Quality Assurance Unit consists of a team of ten experts from diverse fields, including Toxicology, Chemistry, DMPK, Biotechnology, and Environmental Science.
  • QA team members have prior technical experience and extensive knowledge of the subjects they audit.
  • QA auditors undergo exhaustive GLP training conducted by regulatory authorities, external trainers, and in-house experts.

Functions of the Quality Assurance Unit (QAU)

1Study-Based Inspections

  • Review of draft and final study plans.
  • Inspection of critical in-life phases.
  • Evaluation of draft and final reports.

2Facility-Based Inspections

  • Regular audits of processes and facilities.
  • Master schedule audits.
  • SOP/Format audits.
  • Specimen audits before archiving.
  • Audit of contract testing laboratories.

3Additional QAU Responsibilities

  • Reporting inspection findings to Test Facility Management and Study Directors or concerned personnel.
  • Providing GLP regulations training and refresher courses to staff, including new entrants to the QAU.
  • Participating in meetings with sponsors, regulatory authorities, and GLP monitoring authorities.

In-house Audits

  • Comprehensive audits of studies, including study plans, experiments, raw data, and study reports.
  • Regular audits of processes and facilities to ensure ongoing compliance and quality.

Site and Vendor Audits

Conducting audits and pre-placement assessments of facilities at third-party Contract Research Organizations.

Trainings

  • Offering GLP training on various topics, including basic and refresher courses.
  • Providing interpretation of GLP principles.
  • Tailored job-specific training.
  • Conducting compliance case studies.
  • Promoting a quality-by-design approach.

Standard Operating Procedures

  • Preparation and revision of standard operating procedures to ensure they meet GLP standards.
  • Reviewing SOPs for GLP conformity to maintain high-quality standards.

Validation of Computerised Systems

Establishing validation standards and performing thorough validation processes for computerized systems to ensure accuracy and reliability.

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