| Type of Material: | Thesis |
| Title: | Survey of health adult human participants of early phase bioequivalence pharmacokinetic endpoint study in Gujarat state of india |
| Researcher: | Desai Sharad L |
| Guide: | Patel, Nilesh J |
| Department: | FACULTY OF PHARMACY |
| Publisher: | Ganpat University |
| Place: | Mehsana |
| Year: | 2024 |
| Language: | English |
| Subject: | Clinical Medicine | Clinical Pre Clinical and Health | Critical Care Medicine | Pharmacy | Pharmacy | Medical and Health Sciences |
| Dissertation/Thesis Note: | PhD; FACULTY OF PHARMACY, Ganpat University, Mehsana; 2024; 18276011002 |
| Fulltext: | Shodhganga |
| 000 | 00000ctm a2200000ua 4500 | |
| 001 | 455340 | |
| 003 | IN-AhILN | |
| 005 | 2024-09-26 17:01:49 | |
| 008 | __ | 240924t2024||||ii#||||g|m||||||||||eng|| |
| 035 | __ | |a(IN-AhILN)th_455340 |
| 040 | __ | |aGANU_384012|dIN-AhILN |
| 041 | __ | |aeng |
| 100 | __ | |aDesai Sharad L|eResearcher |
| 110 | __ | |aFACULTY OF PHARMACY|bGanpat University|dMehsana|ein|0U-0132 |
| 245 | __ | |aSurvey of health adult human participants of early phase bioequivalence pharmacokinetic endpoint study in Gujarat state of india |
| 260 | __ | |aMehsana|bGanpat University|c2024 |
| 300 | __ | |a10638 KB|dDVD |
| 500 | __ | |aEarly Phase; Bioequivalence; Pharmacokinetic endpoint; Questionnaire; Validation; Face validity; Content validity. |
| 502 | __ | |o18276011002|bPhD|cFACULTY OF PHARMACY, Ganpat University, Mehsana|d2024 |
| 518 | __ | |oDate of Award|d2024 |
| 518 | __ | |oDate of Registration|d2018 |
| 518 | __ | |oDate of Viva-voce|d2024-01-04 |
| 518 | __ | |oDate of Notification|d2024-01-04 |
| 520 | __ | |aAim: Study of healthy adult human participants of early phase bioequivalence pharmacokinetic endpoint study in Gujarat state of India for their demographics, participation details, awareness level, objectives of participation, factors considered for participation, overall participation experience, other people s reasons for not to participate, reasons to withdraw and not to withdraw the consent even willing to withdraw. Method: Newly developed questionnaire was validated by face validity, content validity and pilot study with 50 participants. After having ethics committee approval, validated questionnaire was administered in English, Gujarati and Hindi languages in 1250 participants after taking their written consent to participate. Filled questionnaire of 583 (i.e., response rate of 46.64%) participants were considered for statistical analysis after coding and comparing data by double entry in Microsoft Excel 2013. Statistical analysis was done with SPSS Version: 25.0 and SAS Version: 9.4 for windows for d |
| 650 | __ | |aPharmacy|2UGC |
| 650 | __ | |aMedical and Health Sciences|2AIU |
| 653 | __ | |aClinical Medicine |
| 653 | __ | |aClinical Pre Clinical and Health |
| 653 | __ | |aCritical Care Medicine |
| 653 | __ | |aPharmacy |
| 700 | __ | |aPatel, Nilesh J|eGuide |
| 856 | __ | |uhttp://shodhganga.inflibnet.ac.in/handle/10603/570878|yShodhganga |
| 905 | __ | |afromsg |
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