Greenlight Guru and BSI Life Sciences have joined forces to empower MedTech companies with the tools needed to gather, manage, and store high-quality clinical data. This collaboration accelerates device clearance timelines and expands global market access through the seamless integration of Greenlight Guru's EDC platform with BSI’s CTMS and eTMF solutions.
REQUEST MORE INFOThe joint offerings will allow organizations to:
Streamline Clinical Operations: Integrate Greenlight Guru's rapid study setup (2-3 weeks) with BSI's comprehensive CTMS and eTMF capabilities, ensuring efficient trial management and document handling.
Enhance Data Quality: Leverage electronic Case Report Forms (eCRFs), ePRO, and eCOA to minimize errors and improve data accuracy, supported by BSI's smart data visualization tools.
Ensure Compliance and Security: Access a pre-validated, no-code solution that meets global regulatory standards (ISO 14155, FDA CFR 21 Part 11, EU MDR) and offers robust data protection.
Simplify Integration: Easily connect with existing systems and streamline data sharing between study centers and sponsors, reducing administrative burden.
Maximize Global Market Access: Accelerate device approval processes through unified, compliant, and efficient data management, supported by the expertise of both Greenlight Guru and BSI in the MedTech industry.