๐Ÿ‡ฆ๐Ÿ‡บAustralia

HREC and SSA Approval Delays

2 verified sources

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 ๐Ÿ‡ฆ๐Ÿ‡บ 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.

Evidence Sources:

Related Business Risks

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