None listed
Conditions
Interventions
None listed
Sponsors
No Sponsor
Eligibility
Inclusion criteria
Inclusion criteria: The Principal Investigators who are involved in the Clinical trial with a minimum of 02 years of experience Human Ethics Committee members of Northern Karnataka region Selected Clinical trial participants Pharmaceutical sponsors and their representatives
Exclusion criteria
Exclusion criteria: Declined interest to provide a written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Better understanding on Genetic data reuse for future research to the clinical trial Stakeholders. i.e. Clinical trial protocol reviewers (Ethics Committee members), Researchers/Investigators and Subjects-Study Participants on Pharmacogenic genomic data sharing for future research Development of a Genetic consent model for Genetic study data sharing for future research Timepoint: 02 years | — |
Secondary
| Measure | Time frame |
|---|---|
| Development of a Genetic consent model for Genetic study data sharing for future research Timepoint: 01 year | — |
Countries
India
Contacts
Public ContactMrRevana Siddappa Devarinti
KLE COllege of Pharmacy
Outcome results
None listed