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Audits and Quality Assurance

Ensuring quality and compliance across the full product lifecycle

At Argenta, we are committed to quality at every stage of veterinary product development, from early research to pre-clinical and clinical studies and commercial manufacturing. As an integrated CDO, CRO and CMO partner, we ensure consistent compliance, data integrity and product quality from the molecular level to market readiness. Our sites hold various external confirmations that they comply with the desired quality requirements (ISO 9001, GMP and AAALAC).

Our capabilities include:

  • GMP qualification audits of manufacturers of veterinary non-biologicals/pharmaceuticals, non-immunological and immunological (vaccines) veterinary medicinal products during development and commercial manufacturing
  • GCP facility and process audits including protocols, study conduct/study sites, laboratories, reports, data, statistics and study master files
  • GxP supplier qualification and oversight

Our approach

Our integrated operating model enables quality to be built into program execution—not added as an afterthought. By connecting development, clinical, and manufacturing activities, we:

  • Identify risks early
  • Reduce program complexity and handoffs
  • Ensure globally consistent quality standards
Your advantage
  • Regulatory readiness for global markets (EU, US and beyond)
  • Reliable, inspection-ready data
  • Accelerated development with minimized compliance risk
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