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Clinical Supply Chain Management: Dude, Where’s My Patient Benefit?

September 15, 2021 @ 5:30 pm - 7:30 pm

Clinical Supply Chain Management: Dude, Where’s My Patient Benefit?

Program Speaker:

Dr. Lequina Myles, DRSc, MS, MBA, RAC, PMP, PMI-ACP

Senior Director of Quality Assurance and Regulatory Affairs

Phenomenex (a Danaher Company)



Event Agenda:
Date: Wednesday, 15 Sep 2021
5:30 – 6:00 PM Virtual Networking
6:00 – 6:05 PM Welcome and Announcements
6:05 – 7:05 PM Program Presentation
7:05 – 7:30 PM Q & A

Program Topic:
The objectives of this discussion are to:

  • General Overview of Clinical Supply Chain Management and how it fits into the Drug Development Cycle
  • Understand Operational and Regulatory Landscape of Clinical Supply Chain
  • Overview of Good Distribution Practices
  • Challenges and Opportunities for Clinical Supply Chain (eg, temperature sensitive biopharmaceuticals, cell therapies, gene therapies, alternative distribution models: Direct to Patient)
  • Supply Chain Management during COVID-19

Speaker Biography:
Dr. Lequina Myles, DRSc, MS, MBA, RAC, PMP, PMI-ACP has over ten years of experience within the pharmaceutical and biotechnology industries. Lequina currently works as a Director of Quality Assurance and Regulatory Affairs. Her previous role was Regional Quality Director providing quality oversight for international and domestic life science, medical product, and clinical trial supply chain management and distribution.

Lequina started her career in the Quality Control Biochemistry Laboratories and moved up through the ranks managing and supporting global projects, which increased organizational efficiency, productivity, and improved client retention and strategic partnerships. Also, Lequina has provided expertise in project management, continuous improvement, and training and development to various organizations.

Lequina holds a B.S. in Biochemistry from the University of California, Los Angeles (UCLA) and a Master of Business Administration (MBA) with an emphasis in Project Management from Mount Saint Mary’s University. Lequina also obtained a Master of Regulatory Science and Doctor of Regulatory Science (DRSc) from the University of Southern California. Lequina is a certified Project Management Professional (PMP) and holds a Regulatory Affairs Certification (RAC) in both drugs and devices.

In addition to industry experience, Lequina is an Adjunct Faculty in the MBA Program at Mount Saint Mary’s University teaching project management and serves as a Guest Lecturer at the University of Southern California at the School of Pharmacy.

Lequina is passionate about learning and solving innovative and complex problems. Lequina’s research interests are innovative therapies such as cell and gene therapies and developing clinical and commercial strategies to improve patient access and address unmet medical needs. She also enjoys traveling, mentoring others, and teaching.

Not applicable – This is an online event

Online registration (ends 14Sep2021):
$10 SDRAN Member
$15 Non-Member</p)

For Questions Email: programs.committee@sdran.org


September 15, 2021
5:30 pm - 7:30 pm
Event Category: