Clinical Trial Disclosure
When working with our consultants, you can expect the following:
Active monitoring of the global regulatory landscape and understanding of its impact
Expert level experience working with registry reviewers
Development and implementation of fine-tuning robust, global disclosure programs, including standard operating procedures, style-guides and quality controls
Assessment of your current compliance across global registries
Strategic consulting and project management
Clinical trial registration and disclosure of results in registries such as ClinicalTrials.gov, CTIS/EudraCT, UK, including plain language protocol synopsis and results summaries
Disclosure services offered
Protocol registration
Redaction of study documents
XML development
Gap analysis & strategy
Developing and implementing Disclosure programs, SOPs, and style guides
Results Disclosure
Plain language authoring
General advisory services
Workshops
Technology and software platforms consultation
Disclosure Partnerships
ClaritiDox provides tech-enabled services through partnerships with software-providers
What our clients say
“Moving into my fifth year working with ClaritiDox as a preferred provider in the areas of clinical trial, transparency, regulatory writing, medical writing and anonymization services. I found that the quality of work in addition to the quality of people providing the work is a step above the competition that I've normally dealt with. The team is always very professional, looking to take more responsibility wise, and this has led them to become a trusted partner to externalize and work with. I would highly recommend this team”
Head of Clinical Trial Transparency
- Large Pharma Company