Techsol specializes in providing integrated GxP compliant, ready-to-use software platforms for sponsors to streamline data collection, stakeholder collaboration, oversee business processes and gain insights across the clinical development lifecycle.

CLINICAL DATA MANAGEMENT

Focused on High-Quality Data Generation, Clinical Trials Management and Compliance Oversight

Clinical One

Oracle’s Integrated Platform with CDM, Randomization, and Trial Conduct modules.

AccelClinical

Techsol’s fully-managed ready-to-use CDM and Medical Coding Platform for emerging biopharma.

Oracle CDA

Obtain comprehensive insights on clinical programs, trial progress, site performance and data quality.

Compier PMS

Design, Conduct and Manage Post-Marketing Surveillance Studies across Therapeutic Areas.

Doctor input to Computer

CLINICAL TRIAL MANAGEMENT

AccelCTMS

Leverage our fully-managed CTMS Cloud solution powered by Siebel Clinical.

Establish Clinical Trial Efficiency Using AccelCTMS

  • Leverage a centralized trial management database for all investigators
  • Provide users with relevant and timely information
  • Provision trial information to clinical research associates and managers
  • Enable transparent tracking and reporting of clinical trial activities
  • Facilitate communications to the study team

Oracle RTSM

We can implement Oracle Health Sciences Clinical One Randomization & Supplies Management (ORS) solution to simplify trial randomization, allocate blinded investigational product and improve inventory oversight.

Latest Insights

4 Effective Strategies to Accelerate Site Selection to Activation

Introduction to the site selection process Clinical research organizations (CRO) predominantly rely on the internal networks and investigator database to support a clinical study for a drug. As the clinical sphere continues to expand at a rapid pace, there is an upsurge in demand for clinical trial sites worldwide. CROs are striving for new sites […]

Aggregate Reporting – Significance, Classification and Challenges

Aggregate reports are the cumulative reports in the database that emphasise on evaluation of safety profile and risk-benefit analysis of a drug. Aggregate reporting is the process of compilation and submission of aggregate reports to the regulatory agencies over the period of the product’s life cycle (during pre-marketing and post-marketing phase) to provide a comprehensive [...]

Literature Screening – Process overview, challenges en-route and the scope for automation

Medical and scientific literature is a valuable source of safety information that helps in monitoring benefit-risk profiles and emerging safety issues of medicinal products. Literature screening is conducted to ascertain abstracts and articles that provide crucial information on serious and non-serious Individual Case Safety Reports (ICSR) reports and risk-benefit assessment of a drug. The scientific […]

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