policies and procedures for the acquisition of medical materiel

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C–20. Event 20: MADP Review (DVAL).A review chaired by the chairman, as designated according to paragraph 3-55(3), will be convened to recommendproceeding into full-scale development (Phase II). Recommendations for testing should be included in the review. Theminutes of the review will be provided to the AMDTC for approval. (See events 21 and 22.)C–21. Event 21: Submission of Read Ahead Package.The combat developer (AHS) will submit the finalized MES component listing and IPR minutes in a read aheadpackage to all AMDTC members for review. The ICTP, the prototype packing assessment, logistical analysis, materielfielding plan, and requirements for testing of the prototype MES will also be presented to the AM’D TC for approvalas part of the read ahead package.C–22. Event 22: AMDTC Decision Review.Upon completion of AMDTC staffing, the combat developer (AHS) will formally present the MES to the AMDTC forTSG approval. Approval constitutes type classification of the MES for the AMEDD contingent upon all otherregulatory requirements being accomplished (DA approved FBOIP, QQPRI, and approved requirements document) andinitiates the Production and Deployment Phase. If AMDTC mandates testing of the MES, type classification approval iswithheld pending results of events 23 through 29.C–23. Events 23 and 24: Prototype Testing.Approval of the testing recommendations by the AMDTC will initiate these actions. Testing of MES will normally beaccomplished by CEP Testing or Force Development Testing and Experimentation (FDTE); however, OT may beconducted as required. Policies for conducting these tests are set forth in chapter 5 of this regulation and in AR 71-3.C–24. Event 25: Independent Evaluation Report (IER).The combat developer prepares the IER. The JER provides an assessment of the test results and identifies specificpoints and issues that may need clarification or reevaluation.C–25. Event 26: MADP Review (Full-Scale Development).Significant problems or deficiencies identified during testing, for which the corrective actions will significantly alter thecomposition of the MES, will be resolved by MADP review and approved by the AMDTC.C–26. Events 27 and 28: AMDTC Decision Review.This review is required only when significant changes are recommended by the MADP review, based on testing results.C–27. Events 29 an 30: Type Classification Package Preparation.Approval, and SB 700-20Update. The logistician provides the. type classification documentation support package to theAMEDD Technical Committee. The ’Read for the Record’ document is authenticated and submitted to HQ, DARCOMfor recording and later staffing by DCSOPS. SB 700-20 is updated with the assignment of the permanent LIN to theMES.C–28. Event 31: TOE Update.When the MES has been type classified, assigned Standard UN, and published in SB 700-20, chapter 2, CG, TRADOCwill apply the MES to the TOE in the semiannual consolidated change table (CCT). Based on receipt of the CCT,MACOM will apply MES to MTOE for units under their jurisdiction. These MTOEs serve as authorization for units inthe field to requisition the MES and its component parts.C–29. Event 32: Publication of Doctrine and Training Manuals.The training developer will initiate the publication of these manuals and other supporting literature (i.e., Army Trainingand Evaluation Program ARTEP)) to meet first unit equipped date (FUED).C–30. Event 33: MES Component Standardization.The logistician (USAMMA) will initiate actions to the DMMB to standardize all components to the MES that do notrequire developmental efforts.C–31. Event 34: Publish Supply Catalogs.Based on the final approved MES development listing, and congruent with fielding, USAMMA will publish supplycatalogs.40 AR 40–60 • 15 March 1983
C–32. Events 35 and 36: Assembly/Deployment and Initial Operational Capability (IOC).The mission assignee agency will coordinate the MES assembly program. IOC will be achieved after FUED with thefirst attainment of the capability by TOE unit to employ the new MES effectively.C–33. Event 37: Follow-on Evaluation (FOE).The combat developer and other participants may monitor and evaluate logistical and training support and operationalaspects of the MES program by using FOE, with the initial units receiving the equipment. This feedback will indicateany shortcomings requiring corrective actions.AR 40–60 • 15 March 198341
Page 1 and 2: Army Regulation 40-60MEDICAL SERVIC
Page 3 and 4: HeadquartersDepartment of the ArmyW
Page 5 and 6: Contents—ContinuedSection IIIFUND
Page 7 and 8: Chapter 1INTRODUCTION1-1. Purpose.T
Page 9 and 10: (1) Establish policies, plans, and
Page 11 and 12: (5) Prepare the proper Army require
Page 13: (a) User health hazards cannot be a
Page 16 and 17: 3-8. Phases of the NDI acquisition
Page 18 and 19: Figure 3-1. NDI Acquisition Model F
Page 20 and 21: (13) Provide all documents produced
Page 22 and 23: Figure 3-2. MES Acquisition Flow Ch
Page 24 and 25: . Components of an MES. An MES cons
Page 26 and 27: 4-4. Demonstration and Validation P
Page 28 and 29: a. Demonstrate how well medical mat
Page 30 and 31: Table 5-1Summary Test Matrix (less
Page 32 and 33: When approved, however, the ICTP is
Page 34 and 35: Appendix AREFERENCESSection IAR 10-
Page 36 and 37: MIL STD 1388-1(Logistic Support Ana
Page 38 and 39: MIL STD-785(Reliability Program for
Page 40 and 41: (d) Maintenance concepts.(e) LSAILS
Page 42 and 43: the technical data package, the dra
Page 44 and 45: concept and mission profile of usin
Page 48 and 49: GlossarySection IAbbreviationsAAOau
Page 50 and 51: FBOIPfinal basis of issue planFDAFo
Page 52 and 53: MIMERMinor Medical Equipment Requir
Page 54 and 55: SPEFSingle Program Element FundingS
Page 56 and 57: themselves to test in a non-operati
Page 58 and 59: also describes the training require
Page 60 and 61: y whom OT will be accomplished and
Page 62: Test support unit.The command or ag
Page 66 and 67: 60 AR 40-60 • 15 March 1983 • R
Page 68: USAPAELECTRONIC PUBLISHING SYSTEMOn

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