Trial Design

Trial Design

Study outcomes depend on well designed trials. But you already know that. Lets work together to make sure you do not waste time or money. At Epic we help you:


Establish clear and achievable primary & secondary endpoints


Establish clinical effectiveness and tolerability of treatment


Develop trial protocol to determine appropriate study conduct


Minimize placebo effects and increase assay sensitivity


Prevent costly protocol amendments & enhance resource efficiency


Ensure the safety of the patients and the integrity of the data being collected


Recruit qualified patients that meet clinical trial criteria


Receive clear guidance on how and when to measure and evaluate study endpoints


When a trial is poorly designed the result
is increased bias and large variability in
determining treatment effects.


When a trial is well designed and executed,
statistical analyses can be completed quickly and accurately,
preventing increased bias and variability.

Helping Study Sponsors Succeed

Helping Study Sponsors Succeed

Facility Resources You Need


  • Medical Director
  • Full-time on-site physician
  • Contract physicians
  • PAs/NPs
  • ALCS certified staff
  • Registered nurses
  • Medical Assistants
  • ACRP members – CCRC
  • SoCRA members – CCRP
  • Pediatric Phlebotomists (IV certified)
  • Dietician
  • Pharmacist
  • Regulatory specialists
  • Quality Control / Quality Assurance department
  • Experienced Recruitment & Enrollment department
  • Analgesic-experienced staff
  • Education department
  • Data-entry department
  • ACLS, BLS, HIPAA, CITI, GCP, IATA certified staff
  • Annual Investigator and staff GCP/NIH/SOP training
  • Dedicated Quality Assurance and Data Entry teams
  • Dedicated Marketing / Recruitment / Screening teams
  • Dedicated analgesic study coordinators trained to reduce placebo effects
  • Trained research assistants


  • Ample staff work area and lounge
  • Conference room with web conferencing capabilities
  • Onsite 100-person conference room for larger meetings
  • 6 exam rooms
  • Laboritory
  • Dedicated operating rooms
  • 2 oral surgery suites
  • Dedicated research experienced Anesthesiologists and surgical team
  • 8 private, overnight rooms with cable TV capabilities. Building out to 24 private rooms
  • Patient lounge in the dedicated Phase I unit
  • Individual Male & Female showers
  • Dedicated monitor space with Internet access
  • 24-hour security surveillance
  • Backup generator
  • Large secure drug storage area (temperature controlled)
  • Biosafety hood
  • Secure records retention area on location
  • Acute care bed licensing
  • Pharmacy E license
  • DEA Schedule II-V license


  • Temperature controlled freezers
  • 2 Temperature controlled refrigerators
  • Vital sign equipment
  • 2 Centrifuges (ambient and refrigerated)
  • Biosafety hood
  • Continuous pulse oximetry
  • ECG
  • Crash Cart/Emergency equipment
  • AED
  • Oxygen
  • OR surgical equipment
  • All equipment calibrated annually

You Won’t Waste Time.

You Won’t Waste Money.

We are dedicated to the drug & treatment development process, because we understand how it impacts both sponsors and patients.

Get In Touch

We can't wait to learn more about your study. Let's get to work on a customized strategy today!