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Why Partner with Clintract?

To meet the demands of a challenging global marketplace, pharmaceutical and nutritional supplement companies of all sizes are embracing strategic partnerships to create a cost-efficient blend of internal and external resources that helps them optimize their development programs and product portfolios.  This new approach allows companies to reduce oversight costs and concentrate on their highest priorities – such as product acquisition, and market expansion. The benefits can include significant cost savings, accelerated product development, higher quality, and reduced risk.  To capitalize on those benefits, however, a company must choose the right partner – one with in-depth experience, proven processes, and a complete range of services that are fully enabled by technology.

A unique combination of expertise, resources and technology

Clintract offers a comprehensive network of expertise, clinical resources, and technology within a single organization – a unique combination that maximizes your product development efficiency.  Whatever your requirements, Clintract is right where you need us, delivering proven, integrated solutions across every phase of the product lifecycle… every therapeutic area… and every geographic region.  Our unsurpassed qualifications include:

 

▪ Full range of services in every phase of clinical research development
▪ Scientific and medical expertise across all major therapeutic areas
▪ Utilization of advanced technologies
▪ Clinical and regulatory strategists encompassing the complete development cycle

Clintract continues to create new models of operating excellence and best practices to help our industry partners address key product development challenges.  The proven benefits of Clintract’s integrated approach include:
 

Cost savings – Reduced sponsor oversight, faster study start-up and closeout, and improved study management
 

Accelerated development times – Faster patient recruitment, better site selection, and integrated technology
 

Risk mitigation – Improved data reliability, proven protocols, and greater focus on first-cycle approvals
 

Quality optimization – Standardized processes, improved training, and reduced data redundancy
 

These benefits can cut the cost of a typical Phase III trial by 10-15 percent – savings at a time when cost reductions and accelerated development times are absolutely vital for success in the pharmaceutical and nutritional supplement marketplace.
 

Clintract – The right choice

By selecting Clintract as your strategic partner, your company can leverage our dedication, expertise, innovative technology, and global infrastructure to accelerate the completion of key development milestones, increase efficiency, and reduce the cost of bringing new products to market.  Most important, only Clintract has the experience, flexibility and resources to provide the right combination of biopharmaceutical services and technology for any product development requirement – making us the right partner for today’s difficult global environment.

​Benefits and Advantages of Conducting Clinical Studies:
 

• Corporate Responsibility

• Proof of efficacy
• Product Marketing Material
• Company’s commitment to safety
• Government Patent Protection
• Generate knowledge and evidence
• Demonstrate effectiveness or comparative  

  effectiveness in different populations
• Demonstrate efficacy
• Meet post-marketing commitments
• Monitor long-term safety and safety in

  different populations
• Manage risks and benefits
• Generate data for new indications or

  label extensions

• Obtain or expand market access
• Prove product value through economic or

  quality of life benefits
• Bring scientific information to

  stakeholders sooner
• Enhance the practice of

  personalized medicine
• Understand the natural history of disease

  and treatment
• Generate evidence for product differentiation

  and positioning

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