Meet PHARMExcel at IIS 2023!

The only dedicated conference for medical device investigator initiated study professionals

Register your interest here

Investigator-Initiated Trials are vital for taking new treatments and therapies from bench to bedside. However the processes and the compliance frame work governing clinical studies have become far more complex due to significant changes.

Join our highly interactive roundtable discussion to demystify the challenges in meeting ISO 14155 requirements

Discussion points will include:

  • What are the investigator and site requirements for conducting clinical investigations in accordance with ISO 14155?
  • Who are the key stakeholders that will ensure compliance of the standard? Ie. sponsor, PI, site team, CRO.
  • Do you need to apply different requirements of the standard to different types of IIS?
  • What do sites and investigators see as their biggest hurdle when conducting clinical investigations?
  • Discuss practical ways to ensure investigators and site staff fulfil the requirements of the ISO 14155 standard i.e. site and facility qualification, investigator and site staff training.

What else will you learn at IIS 2023?

We’re excited to be taking part in this 2 day conference, designed to address the legal and regulatory challenges that investigator-initiated research presents to today’s global medical device corporations. We’re looking forward to meeting you in-person at the event for what is expected to be a highly engaging platform that will provide practical insight into transforming scientific strategy into marketing claims, developing publications strategy with an external investigator, using IIS as a tool for pre-market studies, addressing evidence gaps, measuring ROI, how to get the best out of IIS contracts, and the impact of Brexit on clinical studies and trials.

View the full conference agenda

About PHARMExcel

PHARMExcel is an award-winning, full-service Contract Research Organisation (CRO) that genuinely delivers a flexible and innovative approach to clinical trial delivery. The company is recognised for its in-depth knowledge and experience of the clinical research environment, particularly in the UK, and has a network of regulatory and industry associates, allowing it to provide a global reach.

Tel: +44 (0) 2036426654



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