Spiacenti, impossibile trovare dei risultati che corrispondono alla tua ricerca.

È consigliabile provare quanto segue per riuscire a trovare quello che stai cercando:

  • Controlla l'ortografia della ricerca per parola chiave.
  • Utilizza sinonimi per la parola chiave digitata, ad esempio prova “applicazione” anziché “software”.
  • Inizia una nuova ricerca.

Optimize Site Selection

With inconsistent site profile and performance information spread across various systems, finding and enrolling qualified sites is predominately a manual, complicated, and lengthy process.

Select Cloud Service provides a data-driven approach to weighing selection and performance variables to aid in the identification of sites and target populations ideally suited to studies. Open sites on time and meet enrollment targets.

Key Features

Select Cloud Service Benefits

  • Validate site performance to meet enrollment targets
  • Integrate all data sources to create a comprehensive site profile
  • Integrate workflows to complete all site identification and selection activities
  • Reuse site profile data to maximize accuracy of data
  • Utilize workflows to manage CDA, protocol amendments, site identification surveys, and prestudy visits
  • Enable data-driven business decisions and transparency for regulatory compliance and risk mitigation
 

Select simplifies the process of finding investigative sites by ensuring optimal fit and its integrated workflows allow our globally dispersed clinical research teams to collaborate in real-time. Investigate sites can then be quickly setup to enroll trial subjects using Activate.

Kirill Soldatov, Director of Process Improvement, PSI CRO
Learn More

Study Startup Webcasts

How to avoid significant delays in multi-country studies due to EU 536/2014 clinical trial regulation

How to avoid significant delays in multi-country studies due to EU 536/2014 clinical trial regulation

Learn the importance of this regulation and its impact on large multi-country studies.

Bringing patient centricity and scale to decentralized trials

Bringing patient centricity and scale to decentralized trials

Learn how decentralized clinical trials have forced the industry to rethink their approach to study startup and associated regulations.

Moving beyond 10 steps to clinical study startup

Moving beyond 10 steps to clinical study startup

Learn how the traditional steps needed to start clinical trials need to be expanded upon, collapsed, and fit for purpose.

New EU clinical trial regulation

New EU (536/2014) clinical trial regulation set to attract more studies and innovation

The way clinical trials are conducted in the European Union will undergo a major change when this regulation comes into effect in January 2022, which is binding across all member states.

Are CROs prepared for ICH E6 (R3)?

Are CROs prepared for ICH E6 (R3)?

As CROs fight to maintain market share and ensure long-term survival, those capable of critical thinking and proactive planning may be well-positioned to reap the rewards.

How will ICH E8 (R1) and E6 (R3) make clinical trials oversight more efficient?

How will ICH E8 (R1) and E6 (R3) make clinical trials oversight more efficient?

Learn about forthcoming guidance which renews the focus on efficiencies in conducting clinical trials and provide tools to do so - significantly impacting oversight.

How can the accelerated availability of Pfizer-BioNTech's COVID-19 vaccine be replicated?

How can the accelerated availability of Pfizer-BioNTech's COVID-19 vaccine be replicated?

Learn how Pfizer successfully brought a highly effective and safe COVID-19 vaccine to market in under a year, and how these same breakthroughs could be applied to other studies.

How to build productive, strategic sponsor-CRO partnerships

How to build productive, strategic sponsor-CRO partnerships

Learn how trusted collaboration is key to keeping sponsor-CRO partnerships aligned on shared goals.

How to realize the efficiency benefits of ICH E6 (R3) before it's released

How to realize the efficiency benefits of ICH E6 (R3) before it's released

Learn how the focus on efficiency in ICH E6 (R3) will fundamentally change clinical trials.

How machine learning can help improve the operational efficiency of clinical trials

How machine learning can help improve the operational efficiency of clinical trials

Learn how machine learning can help identify and rectify systemic inefficiencies, allowing life science organizations to learn and adapt.

Reducing Complexity in Starting Clinical Trials

Reducing Complexity in Starting Clinical Trials - More Patients, Faster Startup

Learn how the collaboration between Cognizant and Oracle eliminates redundancy for sites and deliver better outcomes from sponsors/CROs.

U-Turn or Norm?

U-Turn or Norm? #NoGoingBack and Decentralized Trials in a post-COVID-19 World

Will the industry embrace this change or revert back to its old ways post-COVID-19?

Vendor Oversight: Ensuring Compliance by Assessing Study Risks

Vendor Oversight: Ensuring Compliance by Assessing Study Risks

Learn how vendor oversight can be implemented end-to-end, ensuring compliance with ICH regulation guidelines.

Is Artificial Intelligence Critical to Improving Efficiencies and Outcomes in Clinical Trials?

Is Artificial Intelligence Critical to Improving Efficiencies and Outcomes in Clinical Trials?

Learn how to gain critical operational insights by using AI/machine learning to transition from subjective decision making.

COVID-19's Impact on the Digital Transformation of Clinical Trials

COVID-19's Impact on the Digital Transformation of Clinical Trials

Learn how digital transformation roadmaps were accelerated to embrace innovative approaches to overcome adversary.

Learning Library

News and Resources

Clinical trials are constantly evolving, with advancements in technology, industry initiatives, regulatory, and process changes. Gain perspective and learn more about these changes in the resources below.

Trending Study Startup Blogs

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