ICON Clinical Research:

• Is a leading multinational CRO
• Provides clinical development services worldwide
• Assigns CRAs to only one project at a time
• Is registered to the ISO 9002 quality system
• Contractually guarantees data quality and timelines
• Provides competitive pricing through a fixed-fee contract

Our areas of therapeutic expertise include the following:

• Anti-infectives
• Antiretrovirals
• Blood products
• Cardiovascular
• Central nervous system
• Dermatology
• Endocrinology
• Gastrointestinal
• Oncology
• Ophthalmology
• Respiratory
• Rheumatology

Our personnel offer many years of expertise in managing multinational clinical studies in a wide range of therapeutic areas. ICON service include:

• Phase II-IV study management
• Global study management
• Pivotal studies for European and US Registration
• Investigator identification
• Central IRB submissions
• Critical document review
• Investigator grant negotiations and administration
• Monitoring activities form pre-study through study closeout
• Medical support including SAE reporting

ICON Clinical Research offers extensive data management, biostatistical, regulatory affairs, medical writing, and quality assurance services as part of a full-service clinical study management program or on a stand-alone basis.

CLINICON is ICON's state-of-the-art central clinical trials laboratory based in Dublin, Ireland. This modern ISO 9002 registered facility supports ICON's multinational programs. CLINICON provides a staff of experts to conduct and analyze a wide range of routine and customized tests. Laboratory services include:

• Biochemistry
• Hematology
• Microbiology
• Serology
• Endocrinology
• Electronic data transfer
• Customized report writing

ICON has offices throughout North America, Europe, and the Pacific Rim. For more information, please visit the ICON Clinical Research home page.

ICON Clinical Research
Elizabeth Thiele, Vice President, US Business Development
212 Church Road
North Wales, PA 19454 USA
Phone: 215-616-3319
Fax: 215-616-8659