Do you only need a consultation?
Maybe a second opinion ?
Or would you want us to take over all your drug development needs in
the Emerging Markets? Or perhaps you want to enter one of the
major markets with your generic?
What about support of your mature marketed products?
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Looking for assistance?
We can help.
Do you need to find qualified investigators and patients for global clinical trials?
More information about PRS...
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This includes
regulatory support of: new chemical entity development, clinical
trials, marketed products, generics, OTC products, medical devices,
as well as regulatory activities related to mergers and acquisitions.
With the expert help of our Scientific Advisory Board,
we offer medical and clinical consulting of various aspects of drug
development.
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Each professional member
of our staff brings on average over 15 years of experience in multinational
pharmaceutical corporations. We offer second opinion to regulatory
questions and decisions taken by other parties, and we assist sponsors
in negotiations with selected regulatory agencies.
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We can also help you market
your pharmaceutical products and medical devices in the Emerging
Markets of Asia Pacific, Latin America, and Central and Eastern Europe.
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info@pharmregservices.com

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