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Challenged by data growth and regulations?

​Regain control of data with a CDW

If the sheer volume of data is slowing down your decision-making, a CDW lets you regain control. By standardizing data and data exchange processes, your business can speed up statistical analysis and respond more efficiently to demands for information. In the pressurized environment of the clinical development process, this can result in a better use of your resources and a quicker time to market.  

At the center of information management strategy 

Critical clinical data are generated, enriched, cleaned, validated, moved, and deleted by employees throughout the company and by CROs. This poses a risk to data quality and to the accessibility of data. To avoid islands of information hindering access to consolidated clinical data, make the CDW the focal point in your information management strategy. This will also support the drive towards standardization.  

A CDW is about far more than it 

Today, regulations have a direct impact on the CDW design: how data ideally is gathered and fed into the system, and how data should be extracted and submitted is directly influenced.  
NNIT’s consultants understand the regulatory demands and how they affect the business and the IT systems supporting the operation. We know that a value-adding CDW is a CDW in which technology and business operations are merged in the CDW design.  
Let us help you take advantage of a structured and standardized approach to data handling which will provide you with a trustworthy data output at all times. 

NNIT's approach to CDW implementation

  • Initial consultancy and analysis  
  • Implementation, GxP validation, and customization  
  • NNIT can also take care of the operation, and offers hosting, application maintenance, a help desk, and functional support. 

NNIT’s CDW framework gives you: 

  • Standardization of processes, data, programs, and output;  
  • Extended utilization of current and historic data;  
  • Cross-trial analysis options;  
  • Expanded capability for crossorganizational collaboration;  
  • Broadened accessibility of clinical data in the organization;  
  • Compliance with industry standards and authority regulations;  
  • Data standards for enhanced export and import capabilities; and  
  • Increased effectiveness and efficiency in the clinical process. 

About NNIT

NNIT provides a broad variety of services to help you meet the demands of life sciences. We understand the complexity of the life science GxP environment, and we have the life science know-how it takes to ensure efficient processes and support full compliance with the authorities.  

 

 

 

 

 

 

NNIT here+45 7024 ​4242nnitcontact@nnit.com ​​​​​​​​​​​​https://dk.linkedin.com/company/nnitNNIT here

 

 

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