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Informa's Clinical Evaluations & Investigations for Medical Devices
21–22 April 2010
Amsterdam, The Netherlands
Speaker: Sunita Prem Ahir, Regulatory Affairs Manager, Devices
Topic: Post Market Clinical Follow-up: Global Requirements
Click here for more information
02-Jun-10
White Paper from Premier Research Reviews how to Optimize Country Selection in Oncology Clinical Trials
28-Apr-10
White Paper from Premier Research Reviews Risk Evaluation and Mitigation Strategies (REMS) and the Impact on Opioid Analgesics
26-Apr-10
Premier Research Pediatric Experts Presented Poster at 2010 ACRP Conference
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21-Sep-10
Transcather Cardiovascular Therapeutics (TCT) 2010
06-Oct-10
PERI's PSURs: Understanding the Requirements for Pre and Post-Approval Periodic Safety Reports
08-Oct-10
2010 ESMO Congress
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