Optimize Clinical Data with Our Expert Data CRO Support

Overcome Healthcare Challenges with Seamless Data CRO Outcomes

In today’s fast-moving healthcare environment, CROs face various challenges like regulatory hurdles and integrating data between payers and providers. Personalizing patient experiences and ensuring data interoperability are also top priorities.

At ACL Digital, we simplify this complexity by offering seamless integration services, boosting data interoperability, and using AI to improve patient outcomes. With our deep healthcare expertise, we help organizations overcome obstacles, streamline operations, and enhance their services for long-term success. We partner with organizations to handle complex data reporting and analysis, making us a trusted ally in driving superior patient care in an evolving healthcare landscape.

Comprehensive

Service Offerings

Cutting-Edge

Technology

Global Reach

and Expertise

Flexible

Engagement Models

Empower Your Clinical Research with Our Data CRO Offerings

Clinical Data Management

Organizing and managing clinical data throughout studies to maintain accuracy, ensuring efficient data collection, analysis, and reporting for regulatory submissions.

Biostatistics

Applying statistical methods to analyze clinical data, providing insights and supporting data-driven decision-making to enhance study outcomes and regulatory approval chances.

Statistical Programming

Developing and validating programs for data analysis, producing high-quality outputs for regulatory submissions and supporting efficient clinical trial processes.

Medical Writing

Crafting comprehensive clinical documents, including study reports and regulatory submissions, clearly communicating study findings to support regulatory approval and scientific publications.

Real World Data (RWD) and Real World Evidence (RWE)

Analyzing real-world health data to generate evidence of treatment effectiveness, supporting informed healthcare decisions and value-based care.

Project Management

Overseeing clinical study timelines, budgets, and resources, ensuring smooth coordination and on-time delivery of complex research projects across teams.

Pharmacovigilance Services

Monitoring drug safety and identifying adverse effects, ensuring patient safety and regulatory compliance through risk assessment and safety data management.

Regulatory Services

Providing regulatory support for clinical trials, ensuring compliance with regional and international guidelines, and assisting with document preparation and submission.

QA Services

Ensuring quality and compliance across clinical processes through regular audits, documentation reviews, and corrective actions to meet regulatory standards.

Business Model to Accelerate Your Clinical Trials

Functional Service Provider (FSP)

Provides specialized support with dedicated governance, a single communication channel, escalation protocols, and quality assurance. Subject Matter Experts ensure domain-specific support.

FSP Governance
Full Service (FSO)
Fully Dedicated FTEs
Activity-Based Contracting
Mixed-Modality Delivery
Escalation Matrix
On-Demand Talent Pool
QA support
Functional SME support

Project Based Services

Offers comprehensive project management with robust Quality Management Systems (QMS), IT infrastructure, domain-trained managers, regulatory compliance, and a QA-focused documentation system.

QMS Infrastructure
Robust IT Infrastructure and Ownership
Project Managers with Clinical Domain Experience
Functional SOPs/WIs
Regulatory Audit Readiness
Dedicated QA Team
Documentation Management System

Global Delivery Centers (GDCs)

Drives and orchestrates large-scale, risk-managed delivery through our global hub networks by bridging consistent quality systems, specialized data experience, and 24/7 execution to fasten up clinical evidence generation.