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논문검색

재심사 대상 의약품의 시판 후 조사 질 관리에 대한 연구

원문정보

The Quality Control of Post-Authorization Study of Re-Examination in Korea

박은자

피인용수 : 0(자료제공 : 네이버학술정보)

초록

영어

BACKGROUND Re-examination system was post-marketing safety measures for drugs in Korea. The objective of this study was to examine experts’ opinions for post-authorization study and current status of quality control of study in pharmaceutical company to improve the quality of post-authorization study of re-examination. METHODS We conducted mail survey for pharmaceutical company (2014. 9. 15-10. 17) and e-mail survey for experts (2014. 10. 1-10. 17). Questionnaires for 29 pharmaceutical companies and for 19 experts were collected and analyzed. RESULTS More than 80% of experts said that quality control of post-authorization study is needed to improve the study, however, many pharmaceutical companies had a difficulty in conducting study. Seventy two percent of companies pointed out low cooperation of survey sites as difficulty in monitoring of post-authorization study. CONCLUSION Quality control of post-authorization study of re-examination system needs to be improved to provide reliable evidence for drug safety.

목차

Abstract
 연구방법
  1. 조사대상
  2. 조사방법 및 조사내용
  3. 통계분석
 연구결과
  1. 응답자의 특성
  2. 재심사대상의약품의 시판 후 조사(사용성적조사 등)의 질 관리
  3. 재심사대상의약품의 시판 후 조사 시 어려운 점
 고찰
 감사의 말씀
 참고문헌
 부록

저자정보

  • 박은자 Eunja Park. 한국보건사회연구원

참고문헌

자료제공 : 네이버학술정보

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