About Us

Thrana- Providing Innovative Solutions for Life Science Industries.

Welcome to Thrana, a key player leveraging profound knowledge and technical prowess to deliver tailored software solutions for the pharmaceutical sector. Thrana's cloud-based drug safety software solutions are meticulously designed to optimize the entire lifecycle of adverse event reporting, risk assessment, and regulatory compliance. Our safety database software is built on a robust architecture, ensuring the utmost data integrity and security. Additionally, our intuitive interfaces contribute to a seamless user experience, facilitating efficient usage and navigation.

Thrana

Request a call back

Thrana's Pharmacovigilance Software -Streamline your drug safety monitoring processes, mitigate risks effectively, and ensure regulatory compliance effortlessly. 

Why chose us

Thrana's Software solution is tailored to elevate your drug safety standards.

Adverse Event Tracking

Tracks and manages adverse events

Regulatory Compliance

Meets global regulatory standards.

Real-time Data Access

Real-time access for prompt decisions.

Customizable Software

Accommodates organizational needs.

Custom Reporting

Automatic generation of reports.

FAQ'S

Increase Operational Efficiency

Thrana takes away the drudgery of pharmacovigilance. It makes the process easier, efficient, saving time and ensuring better returns.

More info

A drug safety database software effectively centralizes and organizes vast amounts of safety-related data, including adverse event reports, medication errors, and product complaints. By providing a single, comprehensive platform for data storage and management, it reduces the complexities associated with manual data handling and improves efficiency in pharmacovigilance operations.

A drug safety database software facilitates compliance with regulatory requirements by enabling timely reporting and documentation of safety-related information. It automates the generation of regulatory reports, such as periodic safety update reports (PSURs) and expedited safety communications, ensuring adherence to regulatory standards and guidelines. Additionally, it maintains comprehensive audit trails of all data modifications and user activities, supporting transparency and traceability in pharmacovigilance processes.

Flexible Data Schema: A drug safety database should allow for the customisation of data fields and schema to align with the unique requirements of different pharmaceutical companies regulatory bodies.

Configurable Workflows: The database should offer configurable workflows that allow users to define and automate various pharmacovigilance processes.

Scalability: As pharmacovigilance databases accumulate large volumes of safety-related data over time, scalability is essential to support growing data storage and processing requirements.

Integration Capabilities: The database should support seamless integration with external systems and data sources, such as electronic health records (EHRs), clinical trial databases, and spontaneous reporting systems.

Request a demo