Value
We will make our track record available to you in the form of our norms.  We will present ourselves to you as your partners in business growth.  We invite you to evaluate us on this basis.  We will do the same.

You will meet with Numoda’s executive Growth Team that mobilizes human and intellectual capital resources for each growth initiative, infusing them with an activist philosophy to meet or exceed plans, and exemplifying Numoda’s passion for partnership with our clients.

To fortify Numoda’s commitment in the service of business results, the growth team manages the projects that move your initiatives to fast and accurate completion.  The leader for your project unifies total resources into a customized client-specific team.

The team will want you to envision them as co-managers of your work with them. Working with this team, you will see the value of our deliverables, which go beyond data and its interpretation, to consultation on business implementation, and market fulfillment strategy.

We look forward to meeting the challenge of your growth.

The value for our clients
Numoda provides our clients with the unique ability to view, access and interact with all the information together in one place, live, throughout the trial. This addresses the needs of the entire clinical trial team to:

• speedily recruit the correct patients
• reduce screen failure rates
  
• improve patient retention
  
• identify the critical aspects of trials earlier
  
• ensure protocol compliance
  
• proactively manage the entire project
  
• provide consistency across data sources
  
• take less time to raise and resolve issues
  
• provide blinded interim results, and the fastest interim analysis/database locks/ submissions.

These may seem like bold claims - in fact, they are actual results.

Come to our Clinical Trial Center and see for yourself. We have actual trial metrics that support each of these statements, and will supply this information during a visit to our trial center.

How this works
In order to optimize your trial, we use direct feeds from all sources of information - the clinical materials suppliers, the labs, specialty labs, the ECG supplier, safety, sites, and others - ALL the data feeds. Since Numoda consolidates all this, we do the processing of information and 24x7 GC project management, with real-time access to all the data. Most people think only about the classic "clinical data", they may not even think about getting the lab data until the end of the study. They are not getting all the other feeds and getting the complete information. We handle the classic information management/data management, get all the feeds, and push this out to trial participants, early, ongoing, throughout the trial.

To run the trial most effectively, Numoda harnesses and consolidates all clinical trial information from CRF, Lab, ECG, IVR, etc. with CTMS - the IRB, payments, monitor visits, etc. Trial management information (enrollment status, site monitoring activities, study materials management, etc.) is readily available, live, during the trial to everyone involved - from site personnel, to project managers, CRAs and Executive Management. Each of these key people is able to make informed decisions based on real-time information and focused on immediate issues, resulting in avoidance of project delays, cost overruns and quality compromises.

Numoda has performed clinical trials and medical device studies globally, in many therapeutic areas, including CNS, Pain, Cancer, Cardiovascular, Infectious Diseases, GI, Orthopedics, Women's
Health and Osteoporosis.

What's Right for You?
We believe that no two outsourcing decisions are the same. Your specific requirements and needs are important to us. We will help you develop unique and sensible ways to improve product development, manage costs, increase data quality and enhance protocol compliance and data consistency. We deliver the right people, processes and technology, with the project methodologies and the staffing horsepower to back them up.

We have found that client needs vary greatly depending on the specific trial and their internal resources. The one thing that all trials share in common is the need for early reports. Numoda is the only company with patented products that can ensure early reporting of ALL trial information. We can set up automated feeds from all participants, early in the process so that all the integrated information is available in live, early reports, throughout the
entire trial.

We consider all the participants who are intersecting with the trial, and what they need. Any trial-related event, be it at a site, at a lab,
at inventory, etc., is immediately recorded, and any authorized team member can be set up to view that data, live. For your trial to be run most effectively, we spend a lot of time understanding who you are and your exact needs. We have a flexible model and can provide outsourcing services for the entire trial, tools for your own team, or we can 'wrap around' your clinical group, or a group with whom you are already working, without adding a layer of cost.

Products featured herein are protected under US Patents: 6,298,347 - 6,834,285. Other patents pending.