Kayode Yusuf

Kayode Yusuf

Company: Sanofi

Job title: Project Lead, ITS Quality Domain Analyst

Bio:

Kayode graduated with a Bachelor of Science in Computer Science from the University of Ibadan and earned a Master of Science in Engineering Management from Tufts University. Kayode has more than 20 years of experience working in Information Technology supporting GxP business areas in various roles at Pfizer and Biogen. He is a certified Project Management Professional, Certified Quality Analyst, and Black Belt six sigma. He has experience on FDA and EMEA regulation, CFRpart11, and Computer System Validation including admin of HP ALM testing management. He has supported and implemented many applications including, but not limited to: LabWare LIMS, Empower, NuGenesis, HP ALM, and TrackWise. In his most recent role at BLUEBIRD BIO, Kayode was working as a Quality Assurance Manager supporting cloud based systems; thus, giving him experience working in a quality organization outside of ITS.

Seminars:

Ask the experts: Morning Q&A + Open Counsel 10:20 am

Let the speakers answer the questions from the audience in this open counsel.Read more

day: Day One

Interactive Panel Discussion: How Can Industry Shape the Standards for Cloud Solutions in GxP-Regulated Environments? 1:45 pm

How have international regulatory standards, and the subsequent interpretation of these guidelines helped or hindered the pharmaceutical industry through transitions onto cloud platforms? What should be the roles and responsibilities of cloud service users and cloud service providers? Which resources should life science companies refer to to maintain data compliance and remain inspection ready?Read more

day: Day One

Best Practice for Cloud Systems in Regulated GxP Environments 9:40 am

Interpreting FDA rules and maintaining CFRPart11 compliant Evaluating a risk-based validation approach Suggestions for good documentation practice and compliance requirementsRead more

day: Day One

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