Please Wait...

LitTrace

Literature Monitoring Tool

LitTrace is a customizable literature monitoring and tracking tool that ensures timely access to reliable and consolidated information on relevant safety-related literature and creates databases for ICSR's and similar compliance reports.

LitTrace can be used to monitor literature relating to:

  • Clinical evaluation
  • Pre-market approval
  • Adverse events reporting

Benefits of LitTrace include:

  • Fully customizable – per client's unique requirements
  • Flexible folder structure – build multiple folders based on product or therapeutics areas (including subfolders)
  • Import third party data – EMBASE, MEDLINE, etc.
  • Simple, easy-to-use tool – for assessment workflow tracking
  • Configurable reporting engine
  • Flexible delivery options – client environment or Bioclinica hosted
  • Central repository – for weekly hits and full-text articles
  • One-stop solution to track full-text article – translation and contract author requests preparation and compliance as required by the FDA, EMEA and other global regulatory bodies

Download our info sheet

ADDITIONAL RESOURCES

LitTrace and PVTrace

Download Info Sheet

Meet the Bioclinica Safety and Regulatory Team: Sukrit Singh, Engagement Manager

Read Blog

Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

Reminder: Today's webinar on Clinical Endpoint Adjudication kicks off at 1 PM Eastern. > https://t.co/1IU9TVFCFA
bioclinica (3 days ago)
In a new go-to-guide on conducting #Alzheimer's clinical trials, @bioclinica experts Joyce Suhy, Marieke Cajal, Luc… https://t.co/SaBFm3L9CL
bioclinica (4 days ago)
Clinical Endpoint Adjudication Webinar. Join us in a live online event this Friday, (6/15) Details & reg. > https://t.co/uBjlgSMnDS
bioclinica (4 days ago)
Clinical Endpoint Adjudication webinar this Friday! Interested in establishing a universal clinical vocabulary to i… https://t.co/uPD992tSaY
bioclinica (5 days ago)
RT @Pints4PDOrlando: Amazingly grateful to @BioclinicaFLA @bioclinica for their super generous donation to @michaeljfoxorg @teamfox in our…
bioclinica (5 days ago)
RT @E_de_Azambuja: ESMO at ASCO2018: please visit booth 5078 if you want more information on ESMO activities and opportunities @myESMO #asc…
bioclinica (2 weeks ago)

Latest Blogs:

Latin America: Benefit from the Right Partner
Removing Risk from Clinical Trial Management System (CTMS) Implementations
Collaboration Between Clinical Operations and the Logistics and Supply Chain Teams is Key to Trial Success
The Value of Protocol Review
CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen