EOM 1352: Fri 7 June 2024, 11:36

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Investigating Outbreaks of Novel Infectious Disease: An International Case Study
Editorial Archive

Investigating Outbreaks of Novel Infectious Disease: An International Case Study

Investigating Outbreaks of Novel Infectious Disease: An International Case Study What can and should be done when lethal infections with epidemic or even pandemic po...
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Serious Adverse Events (SAE) Audit of an Oncology Clinical Trial
Editorial Archive

Serious Adverse Events (SAE) Audit of an Oncology Clinical Trial

Serious Adverse Events (SAE) Audit of an Oncology Clinical Trial Clinical trials are the cornerstone of the development of new medicines. The safety profile of an inv...
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China – Part of the Critical Path in Drug Development in the 21st Century
Editorial Archive

China – Part of the Critical Path in Drug Development in the 21st Century

China – Part of the Critical Path in Drug Development in the 21st Century In the last thirty years the United States has led the world in the field of R&D as it p...
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Tunisia – A Focus on the Clinical Trials Landscape
Editorial Archive

Tunisia – A Focus on the Clinical Trials Landscape

Tunisia - A Focus on the Clinical Trials Landscape Shifting clinical trials to North Africa is an up-to-date consideration for pharma development leaders for a multit...
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FDA Inspection Close Up – Using Strong Process Mapping and Gap Analysis
Editorial Archive

FDA Inspection Close Up – Using Strong Process Mapping and Gap Analysis

FDA Inspection Close Up - Using Strong Process Mapping and Gap Analysis An FDA regulatory inspection is an activity of verification. It serves to give the FDA the as...
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Risk Mitigation and Due Diligence in Overcoming Lost to Follow-up [LTFU] Subjects in a Clinical Trial
Editorial Archive

Risk Mitigation and Due Diligence in Overcoming Lost to Follow-up [LTFU] Subjects in a Clinical Trial

Risk Mitigation and Due Diligence in Overcoming Lost to Follow-up [LTFU] Subjects in a Clinical Trial The term ‘lost to follow-up’ describes a patient who has premat...
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Enhancement of Regulatory Procedures on Medicinal Products in Serbia – Patients Information Requirements
Editorial Archive

Enhancement of Regulatory Procedures on Medicinal Products in Serbia – Patients Information Requirements

Enhancement of Regulatory Procedures on Medicinal Products in Serbia – Patients Information Requirements Providing reliable information on medicinal products to prof...
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Health Economics and Multinational Randomised Controlled Trials
Editorial Archive

Health Economics and Multinational Randomised Controlled Trials

Health Economics and Multinational Randomised Controlled Trials Collecting clinical efficacy and safety data in multinational randomised controlled trials (MNRCTs) ha...
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Editorial Archive

Improving Transition of Investigational Medicines in Alzheimer’s Disease From Phase I To Phase II

Improving Transition of Investigational Medicines in Alzheimer’s Disease From Phase I To Phase II In January 2012, the Obama administration’s Presidential advisory g...
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Cell-based Testing in Central Laboratories
Editorial Archive

Cell-based Testing in Central Laboratories

Cell-based Testing in Central Laboratories Outsourcing is a growing trend in the pharmaceutical industry. Demands for central laboratory testing using complex cell-ba...
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Catalyst: 12th January 2026
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