HREC and SSA Approval Delays
Definition
Biotech clinical trials require parallel HREC ethics approval and SSA at each site, with institutional authorisation dependent on manual submissions to RGOs.
Key Findings
- Financial Impact: 20-40 hours per trial site (at AUD 200/hr = AUD 4,000 - 8,000 opportunity cost)
- Frequency: Per research project or site
- Root Cause: Manual ethics reviews and SSA processes across jurisdictions
Why This Matters
The Pitch: Biotechnology research in Australia ๐ฆ๐บ loses 20-40 hours per trial on HREC/SSA processes. Automation of ethics submissions eliminates this drag.
Affected Stakeholders
Clinical Trial Managers, Ethics Coordinators, Site Investigators
Deep Analysis (Premium)
Financial Impact
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Current Workarounds
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Methodology & Sources
Data collected via OSINT from regulatory filings, industry audits, and verified case studies.
Related Business Risks
TGA CTN/CTA Notification Costs
Biosafety Non-Compliance Fines
Embryo Research Licensing Overhead
TGA Non-Compliance Penalties
Delayed RDTI Tax Incentive Claims
Datenmanipulation und Verstoร gegen Aufbewahrungspflichten in Forschungsvorhaben
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