CTA-Sticky-button.png clinicaltrialsyearbook+button

Content on this page requires a newer version of Adobe Flash Player.

Get Adobe Flash player


Clinical Trial Supply Midwest 2017

12th & 13th September 2017, Chicago, ILLINOIS

This unique event brings together leading pharma, device and biotech professionals from across the Midwest region. After a hugely successful launch event in 2016, the Clinical Trials Supply Midwest Conference will be returning to Chicago for its 2nd edition, with more content and senior level speakers than before. The Clinical Trial Supply stream will also now be run across the full 2 days due to increased demand.

This two-day event will focus on the most pressing issues facing the industry. The event offers a perfect platform for collaborating and building relationships between sponsors and vendors to facilitate the formation of new partnerships and strengthening existing relationships.

Highlights of the 2017 agenda include engaging sessions on GMP best practices for drug delivery; prepping shipments for global locations and navigating new drug developments in China. Along with an interactive panel discussion exploring ways to make your manufacturing relationships successful.

CTS Midwest will be returning on 12th & 13th September 2017. Please get in touch if you are interested in taking part!


Event News

4 reasons to attend Clinical Trial Midwest 2017

1.       Co-located with Outsourcing in Clinical Trials Midwest

Are virtual clinical trials the answer to patient engagement?

Complexities such as patient engagement and retention continue to affect numerous trials within the clinical space. From the initial recruitment process to communications during a trial, patient engagement is crucial to ensuring a trial reaches its enrolment and final participation numbers, as it can be the backbone to validating a trial. 

Who should attend this event?

The Clinical Trial Supply Midwest event offers attendees the unique opportunity to debate and develop practical strategies that will enable their company, whether big or small, to improve the efficiency of its clinical trial supply chain.

Regulations for an effective clinical trials supply chain

With many regulations being updated or introduced to the clinical supply environment, the importance of staying up to date with these regulations and methods to ensure compliance has become crucial to success in the industry. Thus it is essential to limit these potential barriers in order to maintain an effective clinical supply chain.