Streamline your IRB processes with e-IRB — the most comprehensive electronic solution for Ethics Committee management, clinical trial oversight, and regulatory compliance across India.
We are excited to announce that eIRB 2.0 has officially launched and is now in use.
eIRB 2.0 is packed with innovative features designed to streamline your study and enhance your workflow.
Our team is dedicated to making sure the rollout is as seamless as possible for all users.
We'll provide tutorials, user guides, and a dedicated support team ready to assist you.
The official rollout of eIRB 2.0 will begin on 6 May 2025.
We'll be sharing updates leading up to the implementation date.
eIRB 2.0 is designed to improve your experience with powerful features.
e-IRB Digital Applications: Streamlining Ethics Committee Submissions.
This feature provides users with accessible training modules directly through the e-IRB platform, empowering users with educational resources and guidelines specific to the IRB submission process.
A secure, state-of-the-art facility document storage facility for safekeeping of all documents in a digital format, reducing the risk of loss or damage. Ensuring easy retrieval of documents, aiding in efficient record-keeping and reference.
The platform sends timely notifications to all stakeholders involved in the IRB process. Keeps users informed with email and SMS alerts about application status, meetings, and updates reducing delays and improving communication flow.
Audit trails are an essential feature for ensuring transparency and traceability within the e-IRB process. They provide a detailed record of all actions taken within the system, including who performed them and when fulfilling compliance purposes.
e-IRB streamlines the scheduling and documentation of meetings related to the IRB process. Online access to meeting agendas and MoM ensures that all participants are on the same page and can prepare adequately for discussions.
The platform enables a streamlined and simplified process for submitting documents to the IRB. This online submission process reduces paperwork, saves time, and increases efficiency, especially.
Navigate the complexity of clinical trials with ease. Our eIRB system simplifies tracking and submission, making your research journey smooth and efficient.
Speed up your path to discovery. Our eIRB platform expedites the review process, ensuring your research moves forward swiftly and smoothly.
Stay ahead with confidence. Our eIRB system ensures your research adheres to all regulatory standards, keeping you compliant and protected.
Access your research documents anytime, anywhere. Our eIRB platform enhances documentation accessibility, supporting your research needs on the go.
Protect sensitive information with our robust eIRB system. Experience peace of mind knowing your data is secured against unauthorized access.
Preserve your research legacy. Our eIRB platform provides long-term archival solutions, ensuring compliance and safeguarding your work for future generations.
e-IRB offers a wide array of services to streamline and enhance the efficacy of IEC operations.
Simplifies the process of user registration and login ID creation for IECs, sponsors, CROs, and pharmaceutical companies, ensuring secure and personalized access to the system.
Facilitates active participation of IEC members in their respective roles, allowing them to efficiently perform tasks and responsibilities assigned by the IEC through the platform.
Enables the generation and management of various essential IEC records, including Meeting Agendas, Minutes of Meetings (MoM), and decision-making documents, ensuring organized and compliant record-keeping.
Provides comprehensive information on registered Independent Ethics Committees (IECs) by city, state, or country, offering users easy access to crucial data for informed decision-making.
Streamlines the process of submitting and managing clinical trial applications for IEC review and approval. This feature ensures an efficient and organized approach to application handling and compliance.
Provides a robust system for submitting and reporting study progress, updates, and schedules, as well as managing serious adverse events (SAEs) or adverse events (AEs), and protocol deviations, ensuring up-to-date project tracking.
Offers a flexible login facility with unique IDs and passwords, enabling users to access the system from any location at any time, enhancing convenience and operational flexibility.
Incorporates automated features for user account creation, modification, deactivation, and managing access rights, ensuring efficient and secure user management.
Implements an effective communication system, sending timely email and SMS notifications for application uploads, updates, meeting schedules, and other critical alerts, ensuring all stakeholders are well-informed.
