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PRG has forged strategic alliances that offer our clients additional resources vital to the overall
market success of their products/services. We work in concert with medical technology consultants
offering complementary expertise, allowing us to custom-tailor a seamless package of services to
meet each clients' individual needs. Our strategic partners share our "hands-on" approach that
ensures service in a time- and cost-effective manner. Our strategic partners include:
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Based in Southern California,
Strategic Health Resources is an
innovator in ‘value’ analyses for the medical technology industry. SHR’s Evidence of Value™ Model
(EVM) enables technology companies to quantify the clinical and economic benefits of their
technologies within different patient populations, reimbursement systems and cost environments,
and to present its ‘value’ in a format and language customers, regulators and investors understand.
SHR has created a number of groundbreaking health care benchmarking and pricing tools, and
develops market-positioning strategies for companies in the biosciences.
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With offices in France, Netherlands, Germany and Canada,
Medalliance is a consultant
to the pharmaceutical and medical device industries in the European and Canadian marketplaces.
Medalliance's expertise is in epidemiological-need and cost-of-illness assessment, disease
management, health care product medical-economic positioning, reimbursement, marketing,
and support to market introduction and development.
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HRG has experienced medical device professionals to provide the services needed to grow successful
medical device companies. HRG specializes in Marketing, Business Development, Regulatory and Quality
Systems. HRG was founded to assist the small to mid-size medical device companies with issues that are
best solved with experienced people. They focus on solutions and results that maximize your success.
They can be reached at 651-481-9734 or check their web site at
www.horwathrg.com for further information.
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Regulatory Affairs Associates, a community of experienced professionals, provides consulting in
regulatory affairs, biocompatibility, GMP compliance, and clinical trial management. With over 30
years experience, RAA senior associates work in a virtual environment reducing costs and efficiently
manage results for projects including INDs, NDAs, ANDAs, BLAs, 510Ks, IDEs and CE Marks. Discover
the ease of working with experienced regulatory professionals dedicated to creating results. For more
information, visit their web site at
www.regaffairs.net
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