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Paul Starkey, Executive Director, Medical Affairs
Tutorial: Active Query, Case Assessment and Narrative Writing in ClinicalTrials and Postmarketing Pharmacovigilance: Obtaining Quality Data ThroughClinical Expertise - June 22nd
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Session: Case Assessment and Narrative Generation in Pre- andPostmarketing Safety: Clinically Based Active Query Leads to Data Quality -June 23rd
Nermeem Varawalla, Vice President, Scientific & Medical Affairs
Session: Effective Working with Investigative Sites: Essentials forClinical Trial Conduct in the Emerging World - June 23rd
Claudia Senise, Medical Director, Therapeutic Expertise (Latin America)
Session: Serious Adverse Events in Clinical Trials: A Difficult Issuebetween Sites and Sponsors - June 24th
Tim LaCroix, Vice Resident, Engagement Partner
Session: Proof-of-concept Clinical Trials and Achieving Enrollment GoalsThrough Centralized Recruitment Tools: It Is More Important than Ever? - June25th
Also at the DIA conference, PRA experts will present roundtable sessionsat its booth (#830) for invited attendees. Topics include: Effective ClinicalTrial Conduct in Latin America, Maximizing Value of Post-Marketing Research,Effective Clinical Trial Conduct in India and Medical Monitoring Systems andProtocol Waivers.
About PRA International
PRA International is one of the world's leading global clinicaldevelopment organizations, with over 3,600 employees working from offices onsix continents. PRA is committed to reliable service delivery, program-leveltherapeutic expertise, global access to knowledge, with an involved seniormanagement.
To learn more about PRA International, please visithttp://www.prainternational.com, email [email protected] or call our WorldHeadquarters at +1 (919) 786-8200.Charles Schmidt, Director of Operations, Latin America Session: Postgraduation in Clinical Research: Brazil - June 23rd
SOURCE PRA International
