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

Enabling eSource in Clinical Studies to Optimize Trial Quality

Source data is all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial. Electronic data source or eSource is the data that is initially recorded in electronic format in this process. Biopharma and MedTech [...]

Implementing Electronic Consent for Clinical Trial Participation

Industry Background of eConsent In an attempt to address health authority concerns and improve patient confidence, companies and independent industry bodies have experimented with electronic consent (eConsent) using electronic media such as smartphones, laptops, and tablets. Despite positive outcomes, its implementation remained experimental until FDA officially released a guidance in December 2016. Following in FDA’s [...]

Top 4 Trial Design Best Practices for Medical Device Clinical Studies

What drives the growing complexity in medical device clinical trials? The medical devices industry has revolutionized medicine with significant advances in both detection and treatment of diseases. Clinical trials for medical device regulatory approval are designed to produce valid scientific evidence of safety and effectiveness for the intended uses. Moreover, sponsors must consider designing trials [...]

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