Aarogyaline ensures that all specimens are collected following protocols approved by an Institutional Review Board (IRB), either from donors who have given consent or as de-identified remnants. We uphold rigorous ethical policies and employ advanced procedures to maintain the highest ethical standards in all our activities.
- We ensure that clinical materials collected do not disrupt patient care at participating medical institutions.
- Strict measures are in place to safeguard the privacy and confidentiality of volunteers/donors. This includes coding procedures for all materials and associated clinical information to keep the donor’s identity anonymous.
All clinical materials are acquired following approved protocols, with the necessary IRB approval. Our protocols align with current Indian Regulations, as well as HIPAA, and GCP guidelines regarding the protection of human subjects