Best Clinical Trial Management Platform (CTMS + CDMS)

Who we are and What we offer

At CORE CLINICAL SERVICES, we are dedicated to transforming healthcare through innovative digital solutions and unmatched domain expertise. We cater to a diverse clientele, including Pharma companies, CROs, Trial Sites, Clinics, Hospitals, Independent Medical Examiners, and Medico-Legal service providers.

Founded in 2001, CORE CLINICAL SERVICES exclusively serves the healthcare, pharmaceutical, clinical trials, and medico-legal sectors. Our specialties include Clinical Data Management, Clinical Trials Management, Healthcare Data Analytics, Clinical and Medical Summarization, and Plan of Care preparation.

Our Key Services

Tell us your challenges we will resolve them

CDM (CLINICAL DATA MANAGEMENT)

Validated Data Integrity : Deliver a reliable single source of truth for all clinical trial data with our CDM solution.
Automated Reconciliation: Automatically reconcile data discrepancies to maintain accuracy and consistency.
Complete Traceability: Ensure thorough traceability of all trial data, enhancing compliance and oversight.
Streamlined Data Management: Simplify data handling processes, improving efficiency and reducing errors.

CTMS (CLINICAL TRIALS MANAGEMENT SYSTEM)

End-to-End Management: Oversee the entire clinical trial lifecycle from planning to close-out with ease.
Real-Time Analytics: Get real-time visibility into your trials for faster, more informed decisions.
Streamlined Processes: Simplify study planning, budgeting, and day-to-day trial management.
Enhanced Efficiency: Automate workflows, cut down on costs, and improve operational efficiency.
Data-Driven Insights: Leverage powerful analytics and reporting to drive successful outcomes.

CTBM (CLINICAL TRIAL BUDGET MANAGEMENT)

Total Financial Control: Achieve comprehensive oversight of your clinical trial finances with our CTBM solution.
Enhanced Financial Forecasting: Improve your ability to predict costs and allocate resources effectively.
Accurate Budget Management: Manage and adjust study budgets with precision to ensure financial integrity.
Efficient Payment Tracking: Easily track site budgets and payments, streamlining financial operations for your trials.

eTMF (ELECTRONIC TRIAL MASTER FILE)

Cloud-Based Security: Safeguard all your clinical trial documents in a secure, cloud-based repository.
Comprehensive Document Management: Store, manage, and organize study protocols, informed consent forms, investigator brochures, and monitoring reports in one place.
Centralized Access: Enjoy a centralized digital overview for easy access and sharing of all trial documentation.
Seamless Collaboration: Easily share documents across teams, ensuring compliance and efficiency in trial management.

Easy Customization

Tailored to Your Needs: Customize workflows and features to fit your unique trial requirements.
Flexible Configuration: Easily configure settings to align with study protocols and compliance standards.
Adaptable Reporting: Generate custom reports and metrics that reflect your study’s specific needs.
User-Friendly Adjustments: Make changes quickly and intuitively, without technical complexities.

Custom Reporting

Tailored Report Templates: Customize report templates to fit specific trial requirements and maintain branding consistency.
Dynamic Data Visualization: Use intuitive charts and graphs to simplify complex data for quicker insights.
Real-Time Data Access: Generate reports with up-to-date information for timely decision-making.
Comprehensive Filtering Options: Refine report content using advanced filtering and sorting criteria.

ImproWise Platform: Revolutionizing Clinical Trial Management

Unlock the future of clinical trials with ImproWise CTMS + CDM – a powerful, intuitive platform that simplifies trial management, enhances collaboration, and ensures data accuracy for faster, more efficient research.

Benefits of Using ImproWise

Simplify Your Clinical Trial Management and Clinical Data Management

Huge Costs Savings Over 50% of normal costs

Lowers operational costs, and reduces delays and protocol deviations.

Faster Time -to- market Drugs, Devices, Therapies

Accelerates trial workflows, and expedites data analysis and regulatory submission.

All-in-One Integrated Clinical Trial System

Centralizes operations, enhances collaboration, and unifies data management in a single platform.

Improved Efficiency & Productivity

Automates tasks, streamlines workflows, and reduces manual effort.

Better Compliance & Regulatory Standards

Ensures adherence to regulatory requirements, and maintains data integrity and confidentiality.

Real-Time Monitoring & Reporting

Provides instant access to trial data, and enables informed decision-making.

Enhanced Data Quality & Accuracy

Minimizes errors and ensures compliance with regulatory standards.

Streamlined Trial Mgmt

Optimizes workflows, reduces administrative burden, and accelerates trial timelines.

Configurable & Scalable Platform

Adapts to your trial’s unique needs, supports growth, and scales effortlessly with trial expansion.

Why ImproWise

ImproWise offers reliable, accurate, and user-friendly Clinical Trial Solutions.
You can plan, monitor and manage trials effectively, every step of the way.

Secure Web-based access

Accessible from anywhere and at any time through a secure web interface, ensuring data privacy and convenience.

100% Web & Mobile Friendly responsive

Improwise is adaptable to different screen resolutions and different devices and is fully mobile-friendly. Hence no need to have a native App on your mobile.

Dynamic eCRF Design

Ability to design electronic Case Report Forms (eCRFs) dynamically on the fly, often within a few days, a unique and time-saving feature.

Multi-Trial, Multi-Site Handling

Capable of managing multiple trials and multiple sites within a single system and through a single login simultaneously, streamlining trial management.

Dynamic, Database-Driven System

A highly adaptable system driven by a database, requiring minimal customization for different trials.

User-Friendly Query Builder

A highly flexible query builder accessible to non-technical staff, including Clinical Research Coordinators (CRC), doctors, and Principal Investigators, without the need for programming knowledge.

HIPAA Compliant

Ensures compliance with the Health Insurance Portability and Accountability Act (HIPAA) standards for data security and privacy.

Easy Field Customization

Ability to add new fields to accommodate trial-specific requirements with minimal programming effort.

Comprehensive Audit Trail

Audit trailing for every data element entered and changed by CRCs, Quality Assurance (QA) personnel, or Principal Investigators, ensuring data integrity and accountability.