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SSPCC is equally confident working with major pharmas as with start-up biotech and academic ventures.

We provide the following services to our clients:

  • Recommendation of package of preclinical studies needed for new drug applications through to Phase IV regulatory requests
  • Development of Safety Assessment Package, as independent 3rd party consultant to provide unbiased selection of appropriate studies, design, and cost analysis
  • Liaison and project management of CROs, pulling together all the individual studies to centralize, oversee, and streamline the process
  • Coordination and management of documentation for New Drug Applications (NDA) and Investigational New Drugs (IND)
  • Liaison for academic institutions and pharmaceutical companies
  • Independent 3rd party review of Good Laboratory Practices (GLP)
  • Lab planning and budgeting
  • Coaching of new recruits from academia to better transition them to the differing demands of the pharmaceutical industry and regulatory requirements
  • Streamlined processes and procedures
  • Staffing help during cyclical periods of overload

SSPCC is poised to help you secure corporate funding, venture and private equity in addition to the following services:

  • Facilitating corporate partnering between companies
  • Identifying and in-licensing/out-licensing technologies and products
  • Developing and implementing business plans
  • Providing interim business development management for early stage companies
  • Assessing technologies, intellectual property, products and providing valuations
  • Access to capital
  • Developing and implementing product development plans to support licensing approval

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