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Enterprise Services

Clinical Research Excellence

FreeGCP provides comprehensive GCP services aligned with ICH E6(R3). From workforce training to compliance audits, we support research organizations of all sizes with evidence-based solutions.

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Compliance Overview

JD
Compliance Score
98.2%
+1.4%
Active Sites
142
All Operational
Open Findings
3
-2 vs last month
Staff Trained
1,240
99.8% coverage

Quality Indices Trend

6-month rolling average across all active studies

Global
Regional

Top Risk Areas

Last updated: 14 mins agoView Full Report

Live Validation Stream

Protocol v2.4 Approved
Dr. Elena R.2m ago
Site 042 Audit Initiated
System Auto15m ago
SOP-QA-009 Updated
Sarah M.1h ago

Compliance Architecture

FDA 21 CFR Part 11
ICH E6(R3)
EMA Annex 11
GDPR Compliant
ISO 9001:2015
HIPAA Aligned
SOC 2 Type II

Compliance as Foundation for Excellence

In an era of increasing regulatory complexity, rigorous compliance is essential. We view Good Clinical Practice not as a constraint, but as a foundation for operational excellence. Our dedicated services help transform regulatory obligations into systematic quality, supporting efficient timelines and robust data integrity.

GCP Compliance Experts
Customized Implementation
24/7 Global Support

Professional Development Programs

Modern trials require comprehensive, role-specific training. We develop tailored learning programs that align with your SOPs and therapeutic areas. Our curriculum specialists ensure your team develops both knowledge and practical competency.

Clinical Research Pro
ID: GCP-8821-X
VERIFIED
ICH E6(R3) Compliance100%
Data Integrity (ALCOA+)100%
AE/SAE Reporting100%
Certification Issued
Valid through Dec 2026

Comprehensive Compliance Assessment

Our audit team brings deep regulatory expertise to every engagement. We conduct thorough mock inspections that rigorously evaluate your systems, identifying data integrity gaps and process deviations before regulatory review.

MOCK INSPECTION REPORT
REF: AUD-2025-Q1
98
Score
Readiness Status
INSPECTION READY
Risk Level
MINIMAL
Source Data Verification
Informed Consent Process
Protocol Deviation Log
MITIGATED

Strategic Planning Services

We help prevent problems through thoughtful design and planning. Our strategic consultants partner with you on protocol optimization, global site selection, and regulatory pathway planning to support well-designed trials from the start.

STRATEGIC ACCELERATION
Q3 PROJECTION
Time to Market
-30%
Site Efficiency
2.5x
Standard Industry Timeline18 Months
Optimized Strategy12 Months
Launch Expedited

The FreeGCP Standard

A systematic, four-phase engagement model designed to strengthen your clinical operations and support sustainable compliance.

Comprehensive Assessment

We begin with a thorough evaluation of your current operational state, identifying potential risks and opportunities for improvement that require attention.

Solution Design

Our experts design a customized compliance framework aligned with your therapeutic focus, organizational structure, and regulatory requirements.

Dedicated Implementation Support

We provide ongoing collaboration with your team to execute the strategy, ensuring effective adoption of new SOPs and sustainable organizational change.

Validation & Assurance

Rigorous testing evaluates your readiness for regulatory review, helping ensure your organization is prepared and audit-ready.

Work With Us

Let us support your clinical research compliance needs. Contact our team to discuss how our services can help strengthen your operations.