Q-Pharm Pty Limited is a specialised contract research organisation / clinical trial unit which undertakes a broad range of early phase (Phase 1 & Phase 2) clinical trials for clients in the global pharmaceutical and
biotechnology industries.
Our clients tell us that the benefits of conducting clinical trials at Q-Pharm are:
SAVE TIME
- Fast clinical trial start-up (~4-6 weeks from ethics submission to commencement of the clinical trial)
- Frequent dates for ethics submission (40 meetings per year total - local & commercial committee options)
SAVE COSTS
- Time is money - our clinical trials are completed on time and within budget
COMFORT IN WORKING WITH AN ESTABLISHED PROVIDER
- Excellent working relationship with local HREC (submitted, managed and conducted > 300 studies) and commercial HREC (multiple submissions approved in single round of review)
- USA (FDA), Europe (AFSSAPS and AEMPS), and South America (ANVISA) inspected
- Data accepted worldwide by regulators
- Safe location (high level of IP protection, low-risk stable destination)
Specialties
Early Phase and Vaccine Clinical Trials, Healthy Volunteer Clinical Trials, First in Human Clinical Trials, Early Phase Patient Trials
