Sites' Capabilities

  • Working experience with all major CROs and sponsors .
  • Provide multiple, quality sites catering a large diverse demographic patient population ( ohio , Michigan)
  • Ability to conduct Phase I through Phase IV studies
  • Large database of highly skilled and experienced Investigators ( multi therapeutic specialties )
  • Dedicated, full time and highly experienced ICH-GCP, IATA, CITI trained and certified Clinical Research Coordinators
  • Access to large patient populations
  • Centralized contract and budget resolution ( within 48 hrs)
  • Ability to conduct inpatient and outpatient studies
  • Central IRB
  • Established and stable relationships with large public, private and military institutions
  • Track record of consistently meeting or exceeding enrollment goals
  • Aggressive patient recruitment and retention program
  • Expertise to conduct even the most challenging studies
  • Effective and mutually beneficial working relationships with Investigative sites
  • Provide multiple, quality sites
  • Ability to conduct Phase I through Phase IV studies
  • Large database of highly skilled and experienced Investigators
  • Dedicated, full time, and experienced Clinical Research Coordinators
  • Currently we provide coverage in Ohio, but are expanding at a rapid pace and will be adding more locations soon
  • Access to large patient populations
  • Centralized contract and budget resolution
  • Ability to conduct inpatient and outpatient studies
  • Strong working relationships with local and central IRB's and laboratories
  • Established and stable relationships with large public, private and military institutions
  • Track record of consistently meeting or exceeding enrollment goals
  • Aggressive patient recruitment program
  • Expertise to conduct even the most challenging studies
  • Effective and mutually beneficial working relationships with Investigative sites
  • Quality Assurance and Quality Control Team
  • Centralized Source Documentation
  • Training Program
  • Standard Operating Procedures www.cic-america./sops.html
  • Strategically located fully equipped sites
  • Subject Compliance Team

Our staff has experience working with the following pharmaceutical organizations:

  • 3m Pharmaceuticals
  • Abbott Laboratories
  • Abgenix, Inc
  • Allergan, Inc.Alpharma
  • Amgen, Inc.
  • Amylin Pharmaceuticals
  • Astellas Pharma US, Inc
  • .Astra Merck
  • Bayer Corporation
  • Biogen, Inc.
  • Boehringer Ingelheim Pharmaceuticals, Inc
  • Bristol-Myers Squibb
  • Cephalon, Inc
  • Celgene
  • Clinimetrics.
  • Eisai, Inc.
  • Eli Lilly
  • Endo Pharmaceuticals
  • Forest Laboratories, Inc.
  • Gilead Sciences, Inc.
  • GlaxoSmithKline
  • Hoffmann-LaRoche Inc.
  • Insys Therapeutics
  • Metaphor Pharmaceuticals
  • McNeil Pharmaceuticals
  • Merck
  • Nektar Therapeutics
  • Neurocrine Biosciences
  • NeuroGesX
  • Novartis
  • Organon, Inc.
  • Pain Therapeutics, Inc
  • Pfizer
  • Proctor & Gamble Pharmaceuticals
  • Purdue Pharma L.P.
  • Sanofi-Aventis
  • Schering - Plough
  • Sepracor
  • Shire Laboratories
  • Smith-Kline Beecham Pharmaceuticals
  • Squibb Pharmaceuticals
  • Takeda Global Research & Development
  • TAP Holdings
  • UCB Pharma, Inc
  • Valeant Pharmaceuticals
  • Wyeth
  • XenoPort, Inc.

We have worked with the following CRO's:

  • AAI
  • PPDI
  • CATO Research Ltd.
  • ClinTrials Research
  • CTMS
  • Covance
  • Exodon
  • ICON Clinical Research
  • Ingenix
  • Inveresk
  • INC Research
  • Kendle
  • MDS Pharma Services
  • Omnicare
  • PAREXEL
  • Phase Forward
  • Pharmanet
  • PPD
  • PRA
  • Quintiles