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| Collaborates with you in the management of your ethical, high quality paediatric clinical trial |
Welcome to Paediatric Research Consultancy (PRC)Advice and help planning your paediatric clinical trials
From 26 July 2008, Paediatric Regulation EU/1901/2006 mandated that a compliance checked Paediatric Investigation Plan PIP) must be submitted with a drug company's European Marketing Authorisation Application or it will be rejected and the adult or child medicine will fail the licensing process. From 26 January 2009 the same will apply for line extensions. PRC is an independent, ethical, flexible and cost effective service to help you avoid expensive pitfalls commonly associated with testing medicines for children. Metrics of good recruitment, retention and time to market are important aspects of paediatric trial management in a tight economy, so it is important to avoid costly delays. PRC's 17 years of pharmaceutical and academic paediatric trial and 5 years consultancy experience can assist you with the practical, ethical, informed consent/assent, training, planning and operational aspects of your paediatric research. Clients include big and small pharmaceutical companies, biotech, CROs and Government agencies in Europe. SERVICE OVERVIEW:
BENEFITS OF USING PRC EXPERTISE:
Site updated 25 September 2008 |
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