Advice on study design, logistics, conduct and coordination of ethics submission

As a reputable partner to the biopharmaceutical industry, Q-Pharm knows the challenges you face today and are ready to help your trial run in cost-efficient and timely manner.

We provide:

  • Consultation and advice on protocol development
  • Management of ethics submission and approval
  • Participant Information and consent form writing and review
  • Laboratory and data management planning and set-up
  • Vendor coordination (local pathology laboratory and other suppliers)
  • Onsite pharmacy services
    • Development of pharmacy manuals
    • Advice on safety, preperation, handling and storage of IP

Local Human Research Ethics Committee (HREC) Submission and Meeting Dates:

QIMR Berghofer Medical Research Institute HREC

Bellberry Limited HREC

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