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Clinical Trial Initiation

FEASIBILITY ASSESSMENT

Identification and assessment of investigators and sites
Pre-study visits
Selection of investigators and sites
Investigator and site contract negotiation

REGULATORY APPROVALS

Informed consent preparation
Insurance carrier identification and contract negation
Collection of regulatory documents
Application for clinical trial authorizations
Obtaining regulatory approvals from Health Ministry and Ethics Committee

ENROLLMENT PROGRAM

Design of pre-screening program
Study promotion Management
Pre-screening program management
QA of pre-screening program

MISCELLANEOUS

Investigational Medicinal Product Importation
Translation of required documents

EGeen International Corporation

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fax: + 1 650 469 0600

e-mail: egeeninc@egeeninc.com

 

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04074, Kyev,
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