Clinical Trial
Transparency & Disclosure

Achieve your compliance requirements with a trusted partner

Differentiators

Delivery Approach

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We are equipped to mitigate specific challenges that may come with complexity and stringent timelines by customising our approach

Experience and Expertise

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Posted hundreds of records across multiple registries and therapeutic areas. More than 90% of records are registered on Ct.gov without NIH comments on first release

Quality Control

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Thorough QC review of disclosure documents by dedicated QC reviewers/SMEs at every step to ensure high quality and regulatory compliant documents

Complete Package Creation

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Documents marked for redaction/pseudonymisation, Justification sheets, anonymisation report, cover letter, final redacted/anonymised documents

Solutions

Plain Language
Summaries (PLS)
Protocol Registration
& Updates
Results
Postings
Redaction &
Data Anonymization

Plain Language Summaries (PLS)

  • Plain language summary for protocols
  • Plain language summary for clinical trial results
  • Country-specific registration summaries with translations
Find Out More About PLS