Services for Industry

Web based portal - for electronic data capture for clinical trial. -

This is a web based module designed for electronic data capture for clinical trials.

ICTMS - Integrated Clinical Trial Management System for management of trial, project and profile specific access to whole stake holder of the study to perform the task. - This is a web based module design for Integrated Clinical Trial Management of study.

Clinical Data Management:
We have a trained team of Project Managers, Data Managers, Bio-Statisticians, Medical Coders and Data Entry Associates with good understanding of industry standard platforms. We further have a comprehensive suite of well-documented SOPs to address each and every process in our Data Management project lifecycle.
  • 1. CRF Design
  • 2. CDM Plan
  • 3. Database Design
  • 4. Validation
  • 5. Double Data Entry
  • 6. Query Management
  • 7. Quality Control
  • 8. Serious Adverse Event Reconciliation
  • 9. Data Listing
  • 10. Database Lock

Medical Writing:
In clinical trials Medical writing is the most effective document to start and finalize the Clinical trial. The Medical Writers team consists of people who have experience in developing documents in various therapeutic areas such as Dermatology, cardiology, infectious diseases, ophthalmology, diabetes, neuropsychiatry, Gynaecology, Orthopaedic and respiratory disorders. Documents are prepared in accordance with SOPs and templates, and customized as per sponsor specifications Life Research Centre ensure accuracy ,consistency in content and help you write a wide array of documents to support your clinical research at any point in development, including:

  • Product development plans
  • Investigator brochures
  • Trial protocols and Case Report Forms
  • Model informed consent forms and Patients Information Sheet
  • DSMB reports
  • Patient narratives
  • Clinical study reports
  • Manuscripts
  • Literature reviews