W81XWH15D0037

IGF::CT::IGF - MEDICAL PRODUCT RESEARCH AND DEVELOPMENT MULTI-AWARD IDIQ. THIS REQUIREMENT IS FOR ALL NON-INHERENTLY GOVERNMENTAL ASPECTS OF MEDICAL PRODUCT/SERVICE DEVELOPMENT AND LIFECYCLE SUPPORT. TYPES OF TASKS INCLUDE PROJECT MANAGEMENT; TECHNICAL EXPERTISE/ASSISTANCE; STRATEGIC PLANNING; MARKET ANALYSIS; TRAINING; ADMINISTRATIVE ACTIVITIES; PHARMACEUTICAL MANUFACTURING AND TESTING; ASSAY VALIDATION; VALIDATED STORAGE AND SHIPMENT; NON-CLINICAL TESTING; CLINICAL RESEARCH (TO INCLUDE MONITORING; SAFETY PHARMACOVIGILANCE AND SURVEILLANCE, FULL DATA MANAGEMENT, AND BIOSTATISTICAL SUPPORT), REGULATORY WRITING AND SUBMISSION SUPPORT, REGULATORY STRATEGY AND CONSULTATION, QUALITY, INTEGRATED LOGISTICS SUPPORT, EQUIPMENT MAINTENANCE SUPPORT AND INFORMATION TECHNOLOGY IN SUPPORT OF EACH TASK ORDER.