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A Longitudinal Model and Graphic for Benefit-risk Analysis, with Case Study
Breaking News Update: Cutting Edge Statistical Methods in Clinical Development
CDER Electronic Submissions Standards Update
Controversial Guidance, eSource and Standards: How Does It All Fit Together in an eClinical World?
Cross-sector Innovation Brings Tailored Therapies to Patients
Electronic Data Capture (EDC): How Much Quality Is Enough?
Emerging Professionals: Optimize your Transition into the Pharmaceutical Arena
Reference Models and the Framework for the Destruction of Paper: How They Are Changing Our Industry
Globalization of Phase 1: Trends and Challenges
Good Pharmacovigilance Practice in a Global Environment
Hot Topics in Clinical Trial Disclosure (CTD)
Hot Topics in Regulatory Affairs Forum
How Medical Writers Are Improving Global Practice and Collaboration
Leveraging Technology in an Age of Readily Available Information
Meet the Regulators: Helping You Ensure GCP Compliance by Knowing the Most Frequent and Serious Findings
Navigating the Intersection of Outsourcing and Quality Oversight
New Guidances on Quality Risk Management by FDA and EMA: Implications for Industry
The Future of Project Management in the Pharmaceutical Industry: What Competencies Will Be Critical?
Re-energize Your Career!
Rx: A New World in Natural Health Products (NHP)
Status of the Use of Electronic Health Records (EHR) in Clinical Research
Who Owns the Service? Challenges in Collaboration Between IT and the Business