KMR Group


Welcome to KMR Group

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KMR Services

 

KMR focuses on the pharmaceutical and biotechnology companies. The services it offers are based on accumulated data from over 4200 clinical studies conducted by more than 25 pharmaceutical companies and numerous CROs. The data is continuously enriched as new studies are added to the TrialMetrix database.

 

 

Using its proprietary database, TrialMetrix, KMR offers a cutting-edge method for companies to measure their processes and performance against their competitors. Our benchmarking methods encompass quantitative measures such as cycle time, quality and cost indicators as well as qualitative measures.

 

Benchmarking Analysis

 

All analyses are confidential. KMR assesses how a company performs relative to the industry without revealing any data corresponding with a specific company. All data KMR receives from its clients is kept confidential.

   
   
  Clients concerned with optimizing resources can take advantage of KMR's resource management model. KMR uses activity-based process analysis to determine changing workload and resource requirements across the entire range of R&D. This enables clients to effectively evaluate their resource management strategies and determine when they need to outsource or recruit.

 
Another focus is clinical resource management. We have a user friendly resource model that gives managers a powerful tool to project and assess resource needs. It is a flexible application, permitting company planners to run scenarios, adjusting for programs/studies that, for example, are outsourced, do not start on time, or may not begin at all. It portrays results in a variety of ways: by function or role, protocol, program, and period or a combination of those.
   
   
  KMR has compiled detailed enrollment information from thousands of recent protocols conducted globally in all indications. Clients are able to access this information, obtaining a powerful tool to help them more efficiently manage and predict enrollment for specific studies, as well as at more strategic levels where large-scale planning occurs and performance is measured. Depending on the criteria selected, for each protocol the outputs include: subject volume, site volume, subjects per site, subjects per month, length of enrollment, enrollment curves.
   
   
  • R&D Metrics
 

KMR helps companies define and improve their approach to performance metrics, developing KPIs best tailored to the specific context of the company and setting the foundation so that they can be successfully introduced within the company. KMR works with clients to help them effectively: monitor performance according to the metrics, employ the data to demonstrate progress, benchmark performance against the broader industry, and identify areas for improvement.

   
  • CRO Performance
 

KMR collects data (e.g., cycle time, cost, quality) on the CROs a client has recently used or from CRO clients themselves. KMR then evaluates the CRO performance against the industry standard, helping clients understand various CROs strengths and weaknesses and better select and manage CROs. For CRO clients, it highlights areas for improvement and gives a comparison with other CROs.

 

 


KMR provides a detailed analysis of the individual CROs used by a pharmaceutical company, comparing the CROs against: the company's internal performance, the performance achieved by CROs in general, the best in class CRO, pharmaceutical companies in general, and the best in class pharmaceutical company.

 
 

   
   
  • Forums/Common Interest Groups
 

KMR has over 10 years of experience facilitating forums for the discussion of benchmarking information relating to pharmaceuticals. This facilitation is critical in achieving agreed objectives, definitions and common understanding of the results. For example, KMR recently presented data on R&D trends and investment, pharmacogenetics, and clinical resources. The conferences were specifically designed to allow KMR to present data to selected representatives within the pharmaceutical industry. Topics covered by recent forums include: Biologics, Pharmacogenetics, Preclinical Development, Safety Reporting Processes, R&D General Metrics, Portfolio Management, Project Management, Information Technology.




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