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Sites' Capabilities
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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
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