Carrying Out the Research (GCP + GLP)

Whether you are looking for a marketing study, or studies completed to Good Clinical Practice (GCP) or Good Laboratory Practice (GLP) – we can do them all. Our experienced trial coordinators and technicians have meticulous attention to detail in combination with practicality, ensuring credibility and compliance at every stage.

Study Types We Execute:

  • Marketing Studies – Real-world effectiveness demonstrations
  • GCP Clinical Trials – Regulated clinical research studies
  • GLP Laboratory Studies – Controlled laboratory investigations
  • Field Trials – Commercial farm-based research
  • Bioequivalence Studies – Generic product comparisons
  • Safety Studies – Product safety assessments

Our Quality Standards:

  • GCP Compliance – International Conference on Harmonisation (ICH) guidelines
  • GLP Compliance – OECD principles and local regulations
  • Data Integrity – ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate)
  • Quality Assurance – Independent QA oversight
  • Documentation – Comprehensive study documentation
  • Audit Readiness – Preparation for regulatory inspections

Execution Capabilities:

  • Multi-site study coordination
  • Real-time data collection and monitoring
  • Adverse event reporting and management
  • Sample collection and handling
  • Equipment calibration and maintenance
  • Staff training and certification

Ready to start your product development journey? Learn more about our comprehensive product services.

Get in touch

Our team’s often out in the field, so texting works best. Send us a message and we’ll get back to you as soon as we can.

Prefer to call?
You’re welcome to, we just tend to reply faster by text.
You can call us on +61 (0) 409 908 471