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Mr. Tyrrell has over 15 years experience in pharmacovigilance in both Pharma and the CRO industry. With over 16 years of industry experience, Dr. Richter has led PRA's Safety and Risk Management group since 2004. Under Dr. Richter's leadership, PRA opened a new Drug Safety Center in Sao Paulo, Brazil in May of 2009, complementing its existing centers in the US and Germany. PRA's Safety and Risk Management team offers comprehensive services throughout a product's life cycle. PRA provides services to support EU-RMP, FDA-REMS, Annual Safety Reporting, IND Reports and a host of other services. In 2008 alone, PRA processed over 18,000 individual safety reports, submitted 3,000 expedited safety reports to regulatory authorities and contributed to 3 FDA approvals for its clients.
About PRA International
PRA International conducts clinical trials in more than 65 countries across 6 continents and provides services through all phases of clinical development. PRA performs studies in all therapeutic areas, with specialization in Oncology, Neurosciences, Respiratory/Allergy, Cardiovascular and Infectious Diseases. PRA has supported over 2,100 clinical trials through its 36 global offices.
PRA's therapeutic expertise, global reach and project experience, combined with extensive local knowledge and our differentiating PERSONAL ELEMENT enable our project teams to deliver consistent and on time performance for our clients. This unique PRA philosophy - THE PERSONAL ELEMENT - recognizes that true client service comes only from trained, empowered and dedicated employees who are encouraged to use innovation and their personal commitment to accelerate the development lifecycle.
To learn more about PRA International, please visit www.PRAinternational.com, email Endpoints@PRAintl.com or call our Global Headquarters at +1 (919) 786-8200.
SOURCE PRA International
http://www.prainternational.com
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