This course is designed to familiarize participants with the important aspects of Clinical Trials. This overview course gives an opportunity to participants to develop clear and basic understanding about Clinical trials and background of clinical trials which shall be of vital importance while going through actual processes in practice. The course discusses the topics in a lucid way aided by clear and expressive pictorial representations of the concepts and topics. The course covers the topics in multidirectional way and stresses the important points to be remembered while working in GCP regulated environment. This is an online/E-learning course and participants can go for training while pursuing their education or current job.

$ 0 / Indian Rs. 0

Good Clinical Practices are the Global standard that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected. All the Clinical Trials globally are conducted as per the provisions of GCP.

This course is designed to provide participants important aspects of Good Clinical Practices. This course gives an opportunity to participants to develop clear and basic understanding of the GCP. The course discusses the topics in a lucid way aided by clear and expressive pictorial representations of the concepts and topics. The course covers the GCP topics in multidirectional way and stresses the important points to be remembered while working in GCP regulated environment.

$ 50 / Indian Rs. 1499 *
(* Fee in Indian Rupee can only be paid by Demand Draft drawn on any Nationalized/Commerical Indian Bank)

This course is designed to provide participants important aspects of Regulatory Audits and Non compliances during a Clinical Trial. This course gives an opportunity to participants to develop clear and basic understanding about the Compliance of the Regulations and emphasize on the points that might jeopardize the clinical study. The course guides the participants about the approach Regulatory Agency takes while auditing a clinical study along with the consequences for the Non-compliance to the applicable regulations. The course also highlights the common non compliances made by the various key players in clinical trials and also what are major issues to look for while conducting a clinical study.

The course discusses the topics in a lucid way aided by clear and expressive pictorial representations of the concepts and topics.

$ 70 / Indian Rs. 2499 *
(* Fee in Indian Rupee can only be paid by Demand Draft drawn on any Nationalized/Commerical Indian Bank)

This course is designed to provide trainees with a working knowledge of the management of clinical data used in clinical trials and other projects, leading to an academic and professional qualification for Clinical Data Management (CDM). Development of the course involves extensive consultation with the industry. The course is suitable for health information managers, data managers and other health professionals working with, or planning to work with, clinical data and other health databases. The program provides those attending a stimulating and enjoyable opportunity to develop both as individuals and as professionals, increasing their efficiency, effectiveness, capacity and competence, and building on the skills and knowledge gained from valuable work experience.

$ 150 / Indian Rs. 4999 *
(* Fee in Indian Rupee can only be paid by Demand Draft drawn on any Nationalized/Commerical Indian Bank)