From exploratory biology to FDA approval, we optimize processes and technology so our clients can focus on the science and can effectively and efficiently develop new therapies.

Today’s research approaches are impacted by data volume and complexity, new and emerging technology, and the need to share information across the enterprise. And the dynamic nature of the research process, the regulated nature of the clinical process, and their interplay are critical to successful R&D initiatives.

Patient Acquisition and Retention

There’s no easy answer when it comes to patient recruitment, but it is critically important as it advances the science and the treatment of the disease/condition, helps patients receive superior treatment, and supports others with the same condition. We support patient-centered recruitment initiatives and enable Digital impact by leveraging social listening, social channels, and website pre-screening.

Learn how clients leverage digital technologies to recruit patients for clinical trials.

  • Digital initiatives are an important part of the overall recruitment strategy that give the ability to track metrics, analyze data, identify trends, and optimize efforts for maximum ROI.
  • We understand how social listening can help our clients organize and prioritize findings by therapeutic area and develop focused Insights by audience segment.

Precision Medicine

We help companies address the longstanding issue of drug failures which increase the overall cost of development.  We understand how to implement solutions that enable the identification of the right treatment, to the right patient at the right time, in the right dose. This helps refine the long standing practice both quantitatively and qualitatively. 

  • The time is now for companies to take advantage of availability of new technology (e.g. genomic sequencing; data analysis methods).
  • The availability of large quantities of data (e.g. large scale omics projects; RWE), and address the frustration with overall efficacy of drug candidates.

We support patient-centered recruitment initiatives and enable Digital impact by leveraging social listening, social channels, and website pre-screening.

Research Data Management

To protect and defend scientific inventions and intellectual property, while providing traceability to pre-clinical studies, companies need a robust scientific data management strategy. Our team of experts can engage your team to identify and define stakeholder requirements, a technology roadmap, data architecture, and define process controls to achieve organizational goals.

Read about how scientists share data and collaborate.

  • We guide you through the evaluation and selection of technology solutions that meet your specific business needs, ensuring fit within your technology architecture and standards, and that will scale as your business grows.
  • We ensure control of the critical pipeline assets that are essential to advancing your programs and bringing drug candidates into the clinic.

Research Tools and Applications

The research organization is heavily dependent upon software to get their job done efficiently and effectively. We possess deep domain expertise in the research environment, and have extensive experience with many platforms that can be leveraged to increase productivity and decrease costs.

Learn how to reduce the total cost of ownership, decrease risks, and optimize the value of the R&D application portfolio.

  • We have expertise in the selection and deployment and optimization of research systems such as LIMS and ELN whether on premise or in the cloud.
  • We understand the needs of the scientists, and give them the best tools that allow their focus to be on the science.

Clinical Data Management

We support companies by delivering strategies to implement your vision regarding future clinical data, analytics and technology, and business processes. Our solutions identify new data storage that provide compute and analysis technologies, tools for data ingestion, data linage, data catalog and data management of all clinical and operational data. We help establish new data management, data review and data governance processes to provide data transformation for regulatory reporting, to reconcile and clean data using automated discrepancy management workflow 

Read about how data standardization across the portfolio of clinical trials is critical to transparancy.

  • We establish new data management, data review, and data governance processes to provide data transformation for regulatory reporting, to reconcile and cleanse data using automated discrepancy management workflow.
  • We ensure effective validated and non-validated environments, and improve the efficiency for data analytics and the regulatory reporting.