Practical Application of Just in Time Manufacturing in Clinical Trial Supply

Life Sciences, Pharmaceutical, Pharma Manufacturing & Supply Chain,
  • Wednesday, August 19, 2020 | 11am EDT (NA) / 4pm BST (UK) / 5pm CEST (EU-Central).
  • 60 min

We are delighted to invite you to Almac’s upcoming live webinar Practical Application of Just in Time Manufacturing in Clinical Trial Supply.

As biologics and personalized medicines become more realized, the demand to bring these innovative medicines to market effectively and efficiently grows. Sponsors must adapt to these new pressures as they face increased challenges within their clinical supply chain amid COVID-19 and need to think and work in non-traditional ways to meet the demands of niche clinical trials.

Tapping into real life experience, this webinar will discuss the key milestones that impact clinical trial supply and explore the benefits of having a flexible manufacturing, packaging, labelling and distribution solution. Learn how a Just in Time manufacturing approach addresses the changing market dynamics, and redefines global supply chain processes to support sponsors in overcoming the obstacles they face with high value, time sensitive Investigational Medicinal Product (IMP).

Speaker

http://Natalie%20Balanovsky,%20Almac%20Clinical%20Services

Natalie Balanovsky, Just In Time Manufacturing Solutions Manager, Almac Clinical Services

Natalie Balanovsky is the Just in Time Manufacturing Solutions Manager at Almac Clinical Services in Souderton, PA, responsible for stakeholder engagement, implementation and development of Almac’s Just in Time service suite.

Balanovsky has previously held other roles at Almac including Global Project Leader and Project Manager of Distribution, managing Phase I through IV clinical trials of various size and complexity. She has over 15 years of professional experience within Project Management, Business Development, GMP Operations and Quality Compliance for various industries including pharmaceutical, financial and b2b.

She holds a Bachelor of Science degree in Business from Delaware Valley University and earned her Master of Business Administration with concentration in Finance from LaSalle University. She is a certified Project Management Professional and is a Member of the Delaware Valley Chapter of Project Management Institute.

Message Presenter

Who Should Attend?

This webinar will appeal to professionals in pharmaceutical, biotechnology and CRO companies in the following roles:

  • Clinical Trial Manager
  • Clinical Director
  • Supply Chain Management
  • Associate/Senior Project Manager
  • Manager/Director/VP Clinical Operations
  • Logistics Manager/Specialist
  • Vendor Management
  • Global Logistics Manager/Director

What You Will Learn

  • Examine the evolving clinical trial landscape which requires sponsors to be more adaptive to change, specifically amid the COVID-19 pandemic
  • Using real life case studies, examine practical ways Just in Time manufacturing can help mitigate risk, reduce waste and achieve uninterrupted supply
  • Understand the differences between traditional batch manufacturing and Just in Time manufacturing
  • Identify ways to gain operational and budgetary efficiencies whilst ensuring availability and viability for your expensive, temperature sensitive products
  • Gain insight into best practice strategies when planning for a Just in Time approach

Xtalks Partner

The Almac Group

The Almac Group is an established contract development and manufacturing organization providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally. Our innovative services range from R&D, biomarker discovery development and commercialization, API manufacture, formulation development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture. The international company is a privately owned organization that has grown organically over the past five decades now employing over 5,000 highly skilled personnel across 17 facilities including Europe, the US and Asia. Click here to view our facilities. We have a global reputation for excellence built over 50 years of client service, delivering expertise right across the drug development lifecycle and offering a tailored solution to each of our clients. We will be exceptional, always. 

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