Immunodeficiency Syndrome AIDS / Drug Reaction Adverse Event/Adverse Experience / Safety Monitoring Board Food / US National Institutes of Health Data / Abbreviations (sample) ADR AE / Central Laboratory / /
Event
M&A / FDA Phase / /
Facility
LABORATORY EVALUATIONS AND SPECIMEN COLLECTION / /
IndustryTerm
thorough protocols / study protocols / /
MedicalCondition
HIV / Acquired Immunodeficiency Syndrome / AIDS / /
MedicalTreatment
CONTRACEPTION / NATURAL REMEDIES / /
Organization
World Health Organization / RESEARCH ETHICS BOARD/INSTITUTIONAL REVIEW BOARD / Food and Drug Administration / CTN National Centre / Research Organization / DJARS Committee / FDA / US Department of Health and Human Services Good Clinical Practice Human Immunodeficiency Virus / /
Person
QC SAE SMC SOP TPD / Deborah Kraus / / /
Position
Investigator / Related Complex Clinical Investigator / Principal Investigator / / /
Product
Adverse Events Start Medication / CONCOMITANT ALCOHOL AND ILLICIT DRUG / STUDY MEDICATION / Treatment Complete Physical Exam Bloodwork Urine Test Start Medication / New Drug / /
CTN_Protocol_Template_V2-02