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OBJECTIVE:
JUSTIFICATION:
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FIGURE IV-L-1 |
| SCHEDULE AND FUNDING |
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| ANTHRAX VACCINE | ||
| BOTULINUM TOXOID | ||
| PLAGUE VACCINE | ||
| SEB TOXIN VACCINE | ||
| VEE/WEE/EEE VACCINE | ||
| FIELD DEPLOYABLE DIAGNOSTIC KIT | ||

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FIGURE IV-L-2 |
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| VESICANT AGENT COUNTERMEASURES | ||
| REACTIVE/CATALYTIC NERVE AGENT PROPHYLAXES | ||
| REACTIVE TOPICAL SKIN PROTECTANT | ||

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PHASES I AND II |
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OBJECTIVE:
PHASE I - USE CURRENT/NEAR TERM TECHNOLOGIES TO DEMONSTRATE CAPABILITIES AGAINST SOFT, ABOVE-GROUND BIOLOGICAL WEAPON STORAGE FACILITY. PHASE II - USE CURRENT/EMERGING TECHNOLOGIES TO DEMONSTRATE SUBSTANTIALLY IMPROVED CAPABILITIES AGAINST SIMULATED HARDENED, CHEMICAL WEAPON PRODUCTION FACILITIES. JUSTIFICATION: THESE TARGETS HAVE BEEN IDENTIFIED AS PRIORITY TARGETS BY CINCs. |
FIGURE IV-L-3 |
| SCHEDULE AND FUNDING |
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PHASES I AND II |
THIS ACTD DEVELOPS CALCULATIONAL TOOLS, WEAPON EMPLOYMENT TACTICS, DAMAGE ASSESSMENT, AND COLATERAL EFFECTS TOOLS AND INTEGRATES THEM TO PROVIDE THE WARFIGHTER A RAPID, LETHAL TARGETING METHODOLOGY WITH MINIMAL COLLATERAL EFFECTS. THIS REQUIRES THAT THE ACTD PHASES I AND II:
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PHASES III-V |
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OBJECTIVE:
DEVELOP METHODOLOGIES, INTEGRATE, DEMONSTRATE, AND TRANSITION TO USERS A CAPABILITY TO DEFEAT OR DENY USE OF BIOLOGICAL, CHEMICAL, AND NUCLEAR WMD-RELATED FACILITIES INCLUDING C3I LOACTED ON THE SURFACE, SHALLOW BURIED, OR DEEPLY BURRIED TUNNELS. JUSTIFICATION: THESE WMD FACILITIES ARE THOSE THAT HAVE NOT BEEN ADDRESSED IN THE PHASES I AND II PROGRAMS. THEY HAVE UNIQUE TARGETING CONCERNS REQUIRING NEW WEAPON/WARHEAD CAPABILITIES TO ADDRESS DEFEAT WHILE MINIMIZING COLLATERAL EFFECTS. |
FIGURE IV-L-4 |
| SCHEDULE AND FUNDING |
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PHASES III-V |
THESE PHASES OF THE ACTD MUST DEMONSTRATE A CAPABILITY TO IDENTIFY, CHARACTERIZE, TARGET, AND KILL OR DENY USE OF BIOLOGICAL, CHEMICAL, AND NUCLEAR WMD-RELATED FACILITIES WHILE MINIMIZING COLLATERAL EFFECTS RESULTING FROM DAMAGE TO TARGET FACILITIES.
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