Epic Clinical
Clinical Research Consultancy
Epic Clinical Research & Consultancy offers end-to-end consultancy services designed specifically for clinics and small pharmaceutical companies looking to embark on clinical research. Our consultancy service supports you from the very beginning helping secure study opportunities, design robust protocols, navigate regulatory requirements, and manage trial execution ensuring a smooth and successful research journey.
Benefits
• Strategic Study Acquisition:
Benefit from expert market insights and relationship-building to secure study opportunities that align with your capabilities.
• Robust Protocol Development:
Develop clear, comprehensive, and compliant protocols that serve as the blueprint for your trial, reducing ambiguity and risk.
• Regulatory Navigation:
Receive guidance on meeting national and international regulatory requirements (e.g., FDA, EMA, ICH-GCP), ensuring faster approvals.
• Efficient Trial Execution:
Streamline operations with customized recruitment strategies, operational planning, and ongoing monitoring to keep your trial on track.
• Cost & Time Optimization:
Optimize resource utilization and minimize delays through proactive risk management and real-time process adjustments.
How It Works
1. Pre-Study Assessment & Opportunity Identification:
• Evaluate your clinic’s or company’s capabilities and identify suitable clinical trial opportunities.
• Conduct a feasibility study to ensure the project’s applicability and potential success.
2. Strategic Planning & Protocol Development:
• Collaborate with your team to develop a detailed clinical trial strategy and protocol that meets regulatory standards.
• Define study objectives, milestones, resource requirements, and risk mitigation plans.
3. Regulatory & Operational Setup:
• Guide you through regulatory submission processes and obtain necessary approvals.
• Establish operational workflows for patient recruitment, site readiness, and data management.
4. Trial Execution & Monitoring:
• Provide hands-on support during trial initiation, monitoring, and site management to ensure protocol adherence and quality data collection.
• Implement continuous oversight with regular progress reviews and adjustments as needed.
5. Analysis, Reporting & Continuous Improvement:
• Analyze trial outcomes and compile comprehensive reports that detail successes, challenges, and areas for improvement.
• Use lessons learned to refine processes and inform future clinical research initiatives.
Epic Clinical
Why Choose Epic?
- • Proven Expertise: With over a decade of experience and a global track record, our team understands the unique challenges faced by clinics and small pharma companies in clinical research.
- • Tailored, End-to-End Solutions: We customize our consultancy services to your specific needs, ensuring that every aspect of the trial—from acquisition to execution—is managed with precision and care.
- • Regulatory & Operational Excellence: Our deep understanding of regulatory frameworks and operational best practices ensures that your trial not only complies with all standards but is executed efficiently.
- • Collaborative Partnership: At Epic, we believe in working closely with our clients. We become your strategic partner, providing support, guidance, and practical solutions throughout the entire clinical trial lifecycle.
- • Focus on Quality & Patient Safety: Our consultancy service is built on a commitment to delivering high-quality results while prioritizing patient safety and ethical standards at every step.
Get in Touch for Assistance
Do you need help with anything? We can provide you with the most suitable support through our contact page.
