Arena: Outsourcing in Clinical Trials Europe
This European clinical show will provide delegates with practical take-aways and solutions to their most current operational and outsourcing challenges in clinical trials.
Arena: Outsourcing in Clinical Trials East Coast
Join us for a two day event filled with case studies, panel discussion and face to face networking opportunities around clinical operations, technology and innovation, and data management.
PHUSE US Connect
PHUSE’s culture of information sharing and powerful purpose to unite talent ensures our Connect events are a hub for tackling healthcare challenges and advancing the future of life sciences. Join us in Orlando to hear from leading speakers, all in one place, and to level up your career this year and beyond.
Arena: Outsourcing in Clinical Trials DACH
This event will focus upon the operational challenges in clinical development found within Germany, Austria and Switzerland. Over two days, delegates will discuss the common challenges and trends impacting the region, including steps for defining contractual relationships and getting the maximum from external providers, incentivizing good relationships with CROs and constructing defined deadlines.
Arena: Outsourcing in Clinical Trials Nordics
This is the unmissable event that the pharmaceutical, biotechnology, and medical device communities need to come together and discuss strategies for operational success in clinical trials. Combining our OCT, CTS and Medical Devices events, this is the perfect platform for professionals from across a range of clinical trial functions to meet, network, and hear about latest developments.
Arena: Outsourcing in Clinical Trials East Asia
Outsourcing in Clinical Trials East Asia conference is the meeting place for the regional Life Sciences Industry – with over 30 hours of educational sessions and 2 stages this is the event to find ideas and inspiration for your trial needs.
The Conference Forum: Connecting Patient Data in Clinical Trials (Formerly Mobile in Clinical Trials)
This one day event, the day before DPHARM, is centered on connecting the value chain of patient data
(from early drug research to commercialization) with digital technology.
This conference formerly called “Mobile in Clinical Trials” focused on assessing, employing and scaling
mobile tech to help more patients participate and be able to collect patient data remotely.
The conference is expanding to assess all sources of patient data including patient experience data, and how
to best connect the data to optimize clinical trials for all stakeholders.
This conference will include a variety of technological solutions and consider how patient data could be
better utilized in clinical trials.
DIA 2023 Real-World Evidence Conference
In a market that is constantly adapting and adjusting to the needs of the healthcare field, real-world evidence (RWE) is increasingly becoming important for regulatory and reimbursement decision-making. RWE, in relation to the real-world data that is collected in combination with the advancement of artificial intelligence-based analytics platforms, has led to the realtime analysis of data to better understand and gain insights on disease, approaches to treatment, and how to substantiate coverage decisions.
CHI SCOPE Europe Summit for Clinical Ops Executives 2023
Summit for Clinical Trials Operations Executives Europe is a two-day event serving clin ops execs, functional heads, category managers and those responsible for the planning and management of clinical trials. Leaders from large and small pharma,
specialty pharma, biotech, and academic research come together to share best practices and discuss the new era of analytics-driven, patient-centric trials.
SCOPE Summit for Clinical Ops Executives
The SCOPE Summit offers three stimulating days of in-depth discussions in 18 different conferences, 3 plenary keynote sessions, and the ever-popular interactive breakout discussions focused on advances and innovative solutions in all aspects of clinical trial planning, management and operations: Site Selection and Management, Patient Engagement, Recruitment and Retention, Protocol Optimization, Feasibility, Data Strategy & Analytics, Sensors and Wearables, Project Management, Outsourcing, Forecasting, Resource Management and Capacity Planning, Budgeting and Contracting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Post-Marketing Studies, Observational Research, Clinical Supply Chain, and Precision Medicine.