IQVIA RIM Smart. Intelligence, automation and integration.
The MedTech Market Access series kicks off with the most important pain point: change management. We will review, identify and address how best to assess, track and remediate changes across the Safety, Regulatory & Quality (SRQ) processes, and systems in differing global markets.
Change management systems are complex and have challenging design considerations. The process has multiple levers dynamically moving and interacting across the SRQ systems for the same change triggers. A rugged system that allows smooth-bidirectional interactions across SRQ systems along with intelligent workflows is required. Change triggers complex system interactions at multiple folds including product lines, multiple authorities and countries, internal processes and finally design requirements. Designing and aligning such a complex system requirement is no small challenge…
As a participant in this webinar, you will build a better understanding of:
Utilize the experience gained and lessons learned by global trends in handling changes to kickstart your journey towards simplifying your Change Management across your SRQ systems, ensuring ease of implementation, global compliance, and preparedness for future targeted changes.
Michael has around 20 years of knowledge and experience leading localised and global teams in Regulatory Affairs and Quality Assurance and has worked within the Medical and Surgical, Orthopaedic, In Vitro Diagnostic, Diagnostic Imaging, Dental and Urology sectors.
As Senior Director of Product and Strategy within the Technology Solutions business of IQVIA, Michael King is responsible ensuring that the Medical Device solutions have the necessary functionality to support the increasingly complex and diverse global regulations. He is particularly focused on optimizing business workflows through intelligence driven simplification and automation within and across the Safety, Regulatory and Quality functions.
With close to a decade of Technology experience in the Healthcare Platform and Medical Device Industry, Anusha is part of the RIM Smart Product Management team at IQVIA. She drives the mapping of business needs to technical requirements and leads business critical engagements in defining RIM Smart Solutions for MedTech. Prior to IQVIA, she worked as a Regulatory and Quality Engineer at Philips Healthcare and before that spearheaded global product launches at two startups - Consure Medical and Sohum Innovation Lab. Anusha holds a master’s in Electrical Engineering from National University of Singapore with rigorous hands-on experience in the medical device and technology development process from the Stanford-Singapore Biodesign program.
IQVIA RIM Smart. Intelligence, automation and integration.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.