Skip to content

In this on-demand webinar, Eddie Montoya focuses on the many attributes that must be considered to improve your clinical trial efficiency and experience.

You will learn how to use the information you have from the protocol and clinical trial knowledge, along with clinical IRT expertise to ensure that the simple or complex randomization scheme is properly designed and set up to ensure flawless execution. 

As clinical trial success rests on delivering the right clinical treatment at the right place at the right time, the speaker will also illustrate supply chain optimization techniques which can be used as variables within clinical IRT to ensure this basic requirement is met.

This webinar will cover:

  • What excellent clinical IRT looks like in support of your trial
  • Optimizing your timelines
  • Optimizing clinical IRT roll-out and identify the risks and challenges
  • Avoiding pitfalls and rapid course correction – lessons learned

Our Presenters:

Presented by Eddie Montoya, IRT Specialist, Sharp Clinical Services

Eddie Montoya Sharp Clinical Services

Eddie has over 23 years’ experience in the clinical industry and has worked in operations and clinical supplies, directing IRT groups at clinical research organisations (CROs) and managing clinical supply departments at packaging companies. In his previous role, Eddie was director of clinical ancillary management at Fisher Clinical Services and was also director of operations at Covance for 13 years. To date, Eddie has been involved in the management of over 600 clinical studies.

Presented by Suzan Lanz, BS, MBA, Principal, EdisonZ Pharmaceutical Operations Consulting

Clinical IRT Webinar Sharp

Suzan is a seasoned successful biotech professional with over 30 years developing and launching innovative biologics, small molecules and devices in various formulations. Suzan has expertise in early and late stage development projects in various fields such as Oncology, Cardiac Health, Osteoporosis, and Pulmonology. She has demonstrated success in; Project Management, In-Licensing Due Diligence, Operations, Supply Chain, Clinical Quality, Bioanalytical/Analytical Development/Validation, forecasting and strategic planning, systems selection, auditing and cold chain logistics.

To learn more about how Sharp’s IRT platform can help optimize your clinical trial, please contact Eddie Montoya on +1 215-378-5099 or email

Related Resources

Sharp has received Investigational Medicinal Product (IMP) & Wholesale Distribution Authorisation (WDA) licensing approvals to support clinical activities from its facility in The Netherlands.
#clinicalservices #clinicalsupplychain #Brexit

Great to meet new and familiar faces at Pharma & Device Packaging & Labelling Europe 2019 today in Munich. Connect with Scott Forde to learn more about our state of the art facility in Rhymney. @ArenaIntPharma

#pharma #medicaldevices #clinicaltrials

Are you attending Clinical Innovation Partnerships in Berlin next month? Connect with the Sharp team to learn more about our high-speed bottling capabilities.

#clinicaltrials #clinicaltrial #clinicalresearch #clinicaloperations #pharma