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Sunday, March 19, 2023

03-19-2023-1819 - DRAFT

L30 Research Career Programs Loan Repayment Program for Clinical Researchers To provide for the repayment of the educational loan debt of qualified health professionals involved in clinical research. Qualified health professionals who contractually agree to conduct qualified clinical research are eligible to apply for this program.

UNITED STATES OF AMERICA ARMED FORCES

NORTH AMERICA

Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietary choices, dietary supplements, and medical devices) and known interventions that warrant further study and comparison. Clinical trials generate data on dosage, safety and efficacy.[1][2] They are conducted only after they have received health authority/ethics committee approval in the country where approval of the therapy is sought. These authorities are responsible for vetting the risk/benefit ratio of the trial—their approval does not mean the therapy is 'safe' or effective, only that the trial may be conducted. 

https://en.wikipedia.org/wiki/Clinical_trial

ARSENIC MANUFACTURING PROCESSES AND CATABOLIC STIMULANTS

PHOSPHOROUS WHITE MANUFACTURING PROCESSES AND CATABOLIC STIMULANTS

IODINE AND CATABOLIC STIMULANTS

ARTIFICIAL METABOLIC SYSTEMS (NON FECULAR, NON EXCRETORY ; THIN RETAINER)

LEAD WHITE MANUFACTURING PROCESSES AND CATABOLIC STIMULANTS

ACID MANUFACTURING PROCESSES AND CATABOLIC STIMULANTS

CATABOLISM

STARVATION (HUMAN)

POWDERED CELLULOSE

TISSUE AND BODY ENGINEERING (BUILDS)

NUCLEAR ACID MANUFACTURING PROCESSES AND CATABOLIC STIMULANTS

IDENTIFICATION OF NON-APPROVED TISSUE FOR USE IN HUMANS ANIMALS PLANTS (FILLERS, MEAT SLABS, CONNECTIVE TISSUE TYPES, ETC.)

CONSIDERATION OF DEFINITIONS STANDARD PROJECTION MILESTONES GUIDELINES FOR DEVELOPMENT OF TISSUES FOR USE IN HUMANS AND SHELL BUILDS (COMMUNICATION STANDARD, REQUIREMENT COMPETENCE, ETC.)

STANDARD BUILD SHELLS 6'0 30 LBS, IMPLANT FOR BRAIN DEVELOPMENT (OPTION FOR FULL BRAIN TRANSPLANT AND IMPLANT SUBSTITUTION FOR BRAIN ; IMPLANT DEVELOPMENT COMPUTER AND PROGRAMS, PRINTERS FOR IMPLANTS), REPLACEABLE PARTS, SHELL BUILT TO ENABLE MODIFICATION AT HOME (WITH EQUIPMENT SUPPLIES SUPPLIERS INSTRUMENTS ETC.), INCLUDING SHELL REPLACEMENT (EQUIPMENT FOR BRAIN TRANSPLANT INTO NEW SHELL (NO BRAIN IN NEW SHELL) AT HOME TO ENABLE SINGLE PERSON OPERATION, NO ASSISTANCE, NO SPOT NECESSARY, EMERGENCY ASSISTANCE, ETC.), MOBILITY/VISION/LIMBS/RESPIRATORY-CIRCULATORY OR SUBSTITUTE/ARTIFICIAL METABOLIC SYSTEMS (DISSIPATION DEGENERATION NUCLEAR RATE FIELDS MATERIAL USE SCALE/ARRANGEMENT/CODE/STATE/ETC. ETC.), ETC.. PHYSICIANLESS EMERGENCY REPAIR PROCEDURES AND METHODS, OPTIONS (REMEDIATION SUBSTITUTE OR OPTION AUXILIARY/IN ADDITION OR ETC.; IN ADDITION TO USAF PROVISION OF SERVICE TO GENERAL POPULACE TO FACILITATE IMAGE/LIFE/DIGNITY/ETC..). SHOULD BE MADE AVAILABLE TO GENERAL POPULACE, WITHOUT PRECONDITION, LICENSE, FUND, ETC.. FACILITIES MAY BE IMPLEMENTED BY USAF OR FEDERAL GOVERNMENT SUBSIDARY TO SUPPORT EXTRA PROVISION UNITS (VISITORS, PERSONS BETWEEN, EMERGENCIES, OUT OF STATE, ETC.). SHOULD BE AVAILABLE TO EVERYONE, BASIC EQUIPMENT NEEDS AND ASSIGNMENT BY USAF. ALL AGES. DRAFT

CONTINUED ABOVE...BASEFRAME AND BASELINE BIOCHEMISTRY CUSTOM PROFILE ALLOWED, INCLUDING ADVANCED EQUIPMENT FOR SHELL DESIGN (INC. AUTOBUILD, TRANSPIRATION, TRANSMUTATION, IMAGE ESTIMATE RECONSTRUCTION ALGORITHM SPACE, TIME, MATERIALS SELECTION AUTOREFINEMENT, IMPLANT AIDED DESIGN, CALIBRATION/MEASURE/CORRECTIONS/REFINEMENT, IDENTIFICATION OF ERRORS RANGE ETC., ETC.). DRAFT

FOUNDATIONS SHOULD INVOLVE PROPER CONSTITUTION. (DR C USA NAC DOM)


DRAFT

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