It is GSER that change your view style
GSER will serve the community as a resource for the ethical conduct of research and will promote clinical research in India
It is GSER that change your view style
To improve the ethical research for our community by serving as a resource for ethics education, professionalism and compassionate communication in clinical research.
It is GSER that change your view style
GSER-IEC ensures a competent review of all ethical aspects of project proposals received by it in an objective manner free from any bias and influence.
GSER-IECs provide advice to the researchers on all aspects of welfare and safety of research participants after ensuring the scientific soundness.
GSER-IEC overseeing the progress of a clinical study(s) at site by monitoring to ensure that it is conducted, in accordance with the protocol, SOPs, GCP and regulatory requirement(s).
GSER-IEC assist in the development and the education of a research community responsive to local health care requirements.
GSER-IEC review all submitted safety reports and submit their opinion to regulatory bodies as per guidelines.
GSER-IEC protect the dignity, rights and wellbeing of the potential research participants in clinical research.
GSER-IEC is actively engaged in imparting clinical research awareness and training to doctors, clinical research professionals, ethics committee members etc.
GSER-IEC ensure that universal ethical values and international scientific standards are expressed in terms of local community values and customs
GSER-IEC handle issues related to non- compliances, protocol violation, protocol deviations, complaints by the study participants and other stakeholders
GSER has been established by dedicated, experienced clinical research and quality professionals. We believe in working proactively with our customer to bring changes to develop an Ethical mindset. We have a standardized EC review process from submission approval and till study completion through online submission.
We have well defined SOP driven process has been put in place for identification and analysis of study updates, AE & SAE reports, Protocol deviation/ violation and GCP non-compliance which in turn would help organizations that approach us for review and approval of their clinical studies.
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