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CONTENTS


53.


Direct to patient: the rocky road to remote drug delivery in clinical trials Sending investigational drugs directly to study participants is yet to reach its full potential, even in trials that would benefit, argues Reynald Castañeda.


57.


Remote clinical trial monitoring uptake rises but validation questions swirl DCT Adoption Tracker: Clinical Trials Arena reviews the burgeoning trend of remote monitoring.


61. 62.


Chapter 3: Medical devices


The CRO of tomorrow CROs must rise to the challenge of adapting to a changing landscape, according to Excelya.


65.


New UK medical device regulation spells potential trial concerns for some IVD players Forthcoming UK medical device regulations draw some praise from the industry along with caution.


67.


How to extract data insights that could score your next licensing deal or investment Why an integrated and interoperable data collection system could make all the difference.


70.


Patient advisers: could they change the face of medtech trials? Exploring new guidance on integrating patient advisers in medical device clinical studies, and what value this could add.


82.


72.


Empower your next study with a truly unified system Get the lowdown on Axiom Metrics’ e-clinical solutions.


75. 77.


Chapter 4: Decentralised clinical trials and the future


Who and what is at the crest of the clinical trial decentralisation wave? Clinical Trials Arena has used drug trial public information to find out which decentralised approaches are making waves.


SMART digital adherence technology: improving the speed and accuracy of clinical trials WestRock healthcare explains how SMART packaging solutions could help improve health outcomes.


86.


Trial diversity: it’s time to quit talking and start doing As the US takes steps to improve diversity in clinical trials, inequities due to economic factors and race will need to be bridged at institutional levels.


90.


Women’s health clinical trials: breaking down barriers through decentralisation Socioeconomic factors mean women tend to be harder to recruit for clinical trials, but decentralised studies can help ease barriers to participation.


93. Suppliers’ directory


Outsourcing in Clinical Trials Handbook | 5


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