INSIGHTS

Important Clinical Research Insights

SIP integration
Clinical Research Trends

SIP integration developed for KU Cancer Center

Clinical researchers are looking for ways to reduce the operational challenges of clinical trials which can often occur by working with multiple sponsors. Some of these challenges include working with individual sponsor portals, using disparate processes and numerous platforms — each with a unique login credential – which can all lead to increased probability for error and placing patient safety in jeopardy.

As a result, a Shared Investigator Platform (SIP) integration, which can streamline the interaction with multiple sponsors, has become a high priority for many sites.

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Negotiating clinical research budgets
Contracts/Budgets

Developing a Technology Budget During COVID-19

The current pandemic has had a dramatic impact on our personal lives as well as our work lives. And no exception is the impact on clinical research contracts and budgets. In this blog post, we will take a look at how to achieve internal leadership approval – and even sponsor reimbursement – for technology systems, specifically eRegulatory platforms.

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eReg Binder
eRegulatory

The Real Site Regulatory Problem

A lot of work is being invested to ensure research site audit readiness, oversight, and completeness of regulatory files or binders. Unfortunately, there is a lack of understanding if everything is being done to the level of completeness, accuracy and quality that is required. As a result, site regulatory can be a real challenge for Sponsors and CROs.

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#NoGoingBack
Clinical Research Trends

Complion Makes #NoGoingBack Pledge

Complion, Inc. has joined #NoGoingBack, an industry-wide social movement which focuses on keeping in place the clinical research advancements gained during the COVID-19 pandemic.

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Site regulatory standards
eRegulatory

The Case for Standards in Site Regulatory

The development of standards is a proven methodology for efficiency and quality. By implementing an eRegulatory solution, research institutions have the opportunity to standardize clinical trial documentation and processes.

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Disaster preparedness
Disaster preparedness

Developing a Disaster Preparedness Strategy for Your Site

There are limitations to how much property can be protected after a disaster. In the case of clinical research sites, paper documents can burn, or they can be damaged or destroyed by smoke and water. An important consideration for sites is to develop a disaster preparedness strategy with a focus on transitioning to paperless documentation by moving critical study documents to a digital format.

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Request a Demo

See Complion in action!  Request a 30-minute personalized demo and we’ll walk you through how we can deliver industry-leading investigator regulatory solutions for clinical trial sites, sponsors, and CROs.

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Complion news

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