On-demand Sponsored Webcast: Building a Culture of Compliance (On Demand)
Member: $0 | Nonmember: $50
Airtight regulatory compliance is non-negotiable for life science companies.
But there are two very different ways your company can achieve it: by heaping the burden onto your quality and regulatory teams, or by building a business-wide, collaborative culture that knits compliance into all corners.
This webcast is designed to arm you with the insights, tools and best practices you need to put natural, automatic and everyday compliance front and center of your operation.
Registration Fees & Deadlines
Learning Objectives
- Understand the key elements of a modern culture of life science compliance, and how to embed them
- Become constantly audit-ready
- Turn compliance from costly burden into how you do business
- Insulate your business from the risk of recalls and fines
Who Should Attend?
Quality assurance teams Quality managers Regulatory managers Quality directors
Audience Learning Level
Basic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities.
Speakers
Sumatha Kondabulu
Senior Quality Business Partner, Qualio
Sumatha is a senior quality business partner at Qualio, supporting Qualio's regulated life science customers with targeted support to help them optimize their quality systems and embed lasting compliance. She has over 20 years of QA/RA experience across the medical device and pharmaceutical sector, and has built quality management systems for compliance with the FDA QSR, Canada’s Medical Devices Regulations, NIOSH, MDSAP, COFEPRIS, and the EU's MDR, IVDD and IVDR. She holds a Master’s in Chemistry and an advanced certificate in quality assurance management, along with auditor certifications for ISO 13485, 17025 and 9001.
Henry Tri
Relationship Manager & Auditor, TÜV SÜD.
Henry brings over a decade of life science compliance experience right from the coalface, working a string of test, design and process engineering leadership roles before joining TÜV SÜD as lead auditor in 2021.
Henry’s detailed knowledge of GLP and its operational elements combines with deep practical experience of the laboratory environment and its day-to-day operation - giving him unique insights into how to translate compliance requirements and best practice into the fabric of a company culture.
![Regulation of Dietary Supplements and NHPs [3.0 RAC]](https://my.raps.org:443/images/fe351800-9783-45e5-a871-5e951f458074.img?resize=yes)
