id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
bioethics02-18444	Islam, Mohammad Rashedul	Informed consent of human subjects: a review	2014	15	.pdf	application/pdf	8180	353	45	In almost all cases, investigators must document the informed consent process by use of a written consent document (research consent form) signed and dated by the subject or his/her legally authorized representative (or surrogate) and the investigator (or study staff if approved by the PHRC) who obtained the subject’s consent. Sanchez S, Salazar G, Tijero M, Diaz S: Informed consent procedures: responsibilities of researchers in developing countries.	cache/bioethics02-18444.pdf	txt/bioethics02-18444.txt