As life sciences companies face unprecedented pressures from stricter regulations, evolving technologies, and the constant push for cost efficiency, outdated quality systems are becoming a liability. Is your QMS future-proof — or your weakest link? This 30-minute webinar with hands-on demo will highlight five unmistakable signs that your current quality system is overdue for an overhaul and how inaction could put your growth, compliance, and profitability at risk.
After you register, invite your Quality, Operations, and Compliance teammates to also what leading life science companies are doing to modernize their quality systems—and why those who wait risk falling behind in a rapidly evolving landscape.
Sr. Director of Product Marketing and Compliance, Intellect
Tejas is a Biomedical Quality Engineer with 10+ years of experience in medical device development, enterprise software development, manufacturing quality, and business operations and strategy. His Quality experience includes time at Abbott Labs, Halyard Health (now Avanos) and Beckman Coulter (a Danaher Corporation).
Tejas holds an MS in Biomedical/Mechanical Engineering from the University of Bridgeport, a BE in Biomedical/Mechanical Engineering from the University of Mumbai. He's a certified Six Sigma Yellow Belt (CSSYB) and Design Failure Mode and Effect Analysis (FMEA) engineer. He is currently responsible for Intellect’s product lifecycle.
Register for the 30-min Webinar with Live Demo
Wednesday, Feb. 12, 2025 | 12 pm CT
Even if you can't make it, register anyway and receive the replay link.
