Nội dung được dịch bởi AI, chỉ mang tính chất tham khảo
Nghiên cứu Lâm sàng Sau Khi Thuốc Được Chấp Thuận: Cần Gì và Không Cần Gì
Tóm tắt
Bài báo này mô tả các mục đích của các nghiên cứu lâm sàng được thực hiện với các loại thuốc đã được đưa ra thị trường, thường được gọi là "Giai đoạn IV" hoặc "thử nghiệm hậu đăng ký". Các mục đích của những thử nghiệm này được phác thảo, một số vấn đề thiết kế cụ thể cho chúng được thảo luận, và tính phù hợp của việc thực hiện đầy đủ các tiêu chuẩn thực hành lâm sàng tốt trong bối cảnh hậu đăng ký bị đặt câu hỏi.
Từ khóa
#nghiên cứu lâm sàng #thuốc đã được chấp thuận #Giai đoạn IV #thử nghiệm hậu đăng ký #thực hành lâm sàng tốtTài liệu tham khảo
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