01456nas a2200145   4500008004100000245011500041210006900156260001600225300000600241490000600247520097200253653000801225100003201233856004501265       2018                        eng d00aInformed Consent Template by Strategic Initiative for Developing Capacity in Ethical Review. A Good Alternate?0 aInformed Consent Template by Strategic Initiative for Developing  cJanuary 018  a10 v43 a<p class="rtejustify">Obtaining informed consent from (ICF) the participants of a clinical trial, bioavailability and bioequivalence studies, and investigator initiated research consists of two documents; participants’ information sheet and informed consent form. Informed consent is also a mandate for epidemiological and observational studies. It ensure participants autonomy to enroll them in trials and also legally valid for their post trial access and compensation. As a dictum, it should be in English and vernacular language signed by study subjects or their legally accepted representative (LAR).<sup>1</sup> There are valid differences in opinion about amount of information that should be in given consent form. Participant information sheet in too much number of pages is often perceived tedious by the subjects and it is more complex when it comes to countries like India where there is diversity in language.&nbsp;<strong>Read More ....</strong></p>
10aNil1 aChary, Krishnan, Vengadarag  uhttp://ptbreports.org/article/2018/4/1-1