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Nagina Parmar

Dr. Nagina Parmar is Keynote Speaker at Compliance key Inc.She has years of clinical research experience as a certified clinical research professional in academia and hospital. Her expertise as clinical research professional lies in coordinating various Phase I, II and III national and international clinical trials and investigator initiated trials. During her career as CCRP, she was also involved in developing SOPs (Standard operating Procedures), REB SOPs and research elements database. She is an active member of the Society of Clinical Research Associates (SoCRA) and Network of Networks(N2N). As an Adjunct faculty, Dr. Parmar is also involved in teaching Biology, Microbiology, Life Sciences for Clinical practice, and drug development courses at various academic institutions. Her writing appeared in more than 30 journal articles, books and reviews in various national and international journals. As a mentor, Dr. Parmar has provided references and letter of recommendations to assist students with their endeavors. Dr. Parmar has given various career development seminars at University of Toronto to graduates and postgraduates and webinar with Association of Clinical Research Professionals (ACRP).


 Webinar Id: LSHCNP001
 6 months unlimited
 Duration 60 mins
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Investigator initiated trials- What are we doing to ensure human subject protection?

This 1-hr virtual seminar will help you understand the key issues and challenges associated with investigator initiated trials. Investigator initiated trials are very important as they are important connection for the translation of research from bench to bedside. I will discuss the role of sponsor-investigator and ways we can ensure the protection of human subjects in an investigator initiated trials. 

$167 Recorded (6 months unlimited access)
 Webinar Id: LSHCNP002
 6 months unlimited
 Duration 60 mins
Ratings:
No reviews yet!!

Ethical Requirements & Development of Guidelines for Pediatric Trials in Developing Countries

This 1-hr virtual seminar will help you understand the key ethical issues and challenges associated with pediatric studies in developing countries. Pediatric populations in developing countries are extremely vulnerable participants in clinical research. I will discuss some of the key ethical issues and challenges associated with pediatric studies in developing countries and suggest how these can be addressed.

$167 Recorded (6 months unlimited access)


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