Socrate - Guides d'étude, Notes de cours & Résumés

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Moet jij leren over Freud, Plato of Socrates? Alle literatuur nu in één samenvatting. Très apprécié
  • Moet jij leren over Freud, Plato of Socrates? Alle literatuur nu in één samenvatting.

  • Resume • 113 pages • 2024
  • Vind je geschiedenis maar niks, maar moet je het vak helaas toch volgen? Of vind je het juist heel interessant en wil je er meer over weten? Dan is deze samenvatting bedoeld voor jou. Alle literatuur is erin verwerkt, zodat je je optimaal kan focussen op het leren en maken van mindmaps.
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SOCRA CCRP ACTUAL EXAM 300 QUESTIONS AND CORRECT DETAILED ANSWERS TOP RATED VERSION FOR 2024-2025 ALREADY A GRADED WITH EXPERT FEEDBACK|BRAND NEW|REVISED Très apprécié
  • SOCRA CCRP ACTUAL EXAM 300 QUESTIONS AND CORRECT DETAILED ANSWERS TOP RATED VERSION FOR 2024-2025 ALREADY A GRADED WITH EXPERT FEEDBACK|BRAND NEW|REVISED

  • Examen • 53 pages • 2024 Très apprécié
  • SOCRA CCRP ACTUAL EXAM 300 QUESTIONS AND CORRECT DETAILED ANSWERS TOP RATED VERSION FOR ALREADY A GRADED WITH EXPERT FEEDBACK|BRAND NEW|REVISED
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SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide
  • SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide

  • Examen • 356 pages • 2023
  • SOCRA EXAM PREP | 2023 Update | Questions and Verified Answers| Highly Rated Guide Q: What 4 aspects of a trial should a sponsor focus on when monitoring for compliance per 21 CFR 312.56? Answer: 1) Progress of investigations under IND 2) Secure compliance or discontinue investigators that are not compliant and notify FDA 3) Review safety/effectiveness of drug and report safety issues to FDA + make annual reports or progress 4) Notify FDA, all IRBs and all investigators if drug presen...
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CCRP SoCRA Exam Latest Update Rated A
  • CCRP SoCRA Exam Latest Update Rated A

  • Examen • 12 pages • 2024
  • CCRP SoCRA Exam Latest Update Rated A 21 CFR Part 11 Electronic Records; Electronic Signatures 21 CFR Part 11 Subpart B Electronic Records 21 CFR Part 11 Subpart C Electronic Signatures 21 CFR Part 50 Protection of Human Subjects 21 CFR Part 50 Subpart B Informed Consent of Human Subjects 21 CFR Part 50 Subpart D Additional Safeguards for Children in Clinical Investigations 21 CFR Part 56 Institutional Review Board 21 CFR Part 56 Subpart B Organization and Personnel 21 CFR Part 56 Subpa...
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Test Bank for Think with Socrates Guide to Critical Thinking 1st Edition Herrick/ All Chapters 1 - 14 / Full Complete 2023 Test Bank for Think with Socrates Guide to Critical Thinking 1st Edition Herrick/ All Chapters 1 - 14 / Full Complete 2023
  • Test Bank for Think with Socrates Guide to Critical Thinking 1st Edition Herrick/ All Chapters 1 - 14 / Full Complete 2023

  • Examen • 239 pages • 2023
  • Think with Socrates Guide to Critical Thinking 1st Edition Herrick Test Bank Test Bank for Think with Socrates Guide to Critical Thinking 1st Edition Herrick/ All Chapters 1 - 14 / Full Complete 2023
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SOCRA EXAM 2024 -25 WITH 100% ACCURATE SOLUTIONS
  • SOCRA EXAM 2024 -25 WITH 100% ACCURATE SOLUTIONS

  • Examen • 51 pages • 2024
  • SOCRA EXAM 2024 -25 WITH 100% ACCURATE SOLUTIONS Electronic signature are currently accepted for any and all records, paper or electronic form. True or False? - correct answer False. The general provisions for electeonic signature criteria apply to records that are i. Created, modified, maintained, archived, retrieved, or transmitted, in electronic form ii. The criteria do not apply to paper records that are or have been transmitted by electronic means. If the electronic records m...
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SOCRA EXAM PREP | 2024 / 2025 Newly Updated | Questions and Verified Answers | Highly Rated Guide
  • SOCRA EXAM PREP | 2024 / 2025 Newly Updated | Questions and Verified Answers | Highly Rated Guide

  • Examen • 675 pages • 2024
  • SOCRA EXAM PREP | 2024 / 2025 Newly Updated | Questions and Verified Answers | Highly Rated Guide Q: What 4 aspects of a trial should a sponsor focus on when monitoring for compliance per 21 CFR 312.56? Answer: 1) Progress of investigations under IND 2) Secure compliance or discontinue investigators that are not compliant and notify FDA 3) Review safety/effectiveness of drug and report safety issues to FDA + make annual reports or progress 4) Notify FDA, all IRBs and all investigators if drug pr...
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SOCRA CERTIFICATION EXAM QUESTIONS AND CORRECT  ANSWERS VERIFIED BY EXPERTS |ACCURATE ACTUAL EXAM  WITH FREQUENTLY TESTED QUESTIONS |ALREADY A  GRADED |GUARANTEED PASS |LATEST UPDATE
  • SOCRA CERTIFICATION EXAM QUESTIONS AND CORRECT ANSWERS VERIFIED BY EXPERTS |ACCURATE ACTUAL EXAM WITH FREQUENTLY TESTED QUESTIONS |ALREADY A GRADED |GUARANTEED PASS |LATEST UPDATE

  • Examen • 51 pages • 2024
  • SOCRA CERTIFICATION EXAM QUESTIONS AND CORRECT ANSWERS VERIFIED BY EXPERTS |ACCURATE ACTUAL EXAM WITH FREQUENTLY TESTED QUESTIONS |ALREADY A GRADED |GUARANTEED PASS |LATEST UPDATE
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