Our Services

Expert support for all of your Disclosure needs​

Document Redaction and EU Policies

Meeting Global Registry Requirements

Have a new clinical trial about to begin enrollment? Has one just completed? The clock has started! With global registries on the rise and registration compliance increasingly in the spotlight it's hard to know where to begin improving on, supporting, or even starting your disclosure process.

There are many paths to successful compliance but the key to reaching your goal efficiently and effectively is having experienced people to guide you through the process. 

Redaction, anonymization, data sharing... what does it all mean and how do you ensure you are doing what you need to in order to meet the requirements?

Our rigorous redaction process supported by adaptive search technology means you can feel confident in the quality of the finished document.

If you struggle with supporting your data sharing requests, our robust online tracking solutions help you organize and plan


  1. Clinical Trial Registration
    Registration and results disclosure services to meet European, US and international regulatory requirements
  2. Online Tracking Solutions
    Easy to use platforms for tracking disclosure and data sharing projects with dashboards, metrics and more
  3. Document Redaction
    Clinical document redaction and intelligent automation. Document by document redaction to full EMA support services including anonymization report, justification table and cover letter
  4. SAS/XML
    SAS programming and XML transformation to support disclosure and transparency efforts
  5. Medical Writing
    SOP and clinical document writing including Technical and Lay Summaries of Trial Results
  6. Pharmacovigilance
    Market Research and Patient Support Program, Pharmacovigilance process consulting and tracking technology