Converge or Be Purged: IDMP Product Standardisation Deadline Looms
The Identification of Medicinal Products (IDMP) is a set of standards defined by the International Organization for Standardization (ISO). The…
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Electronic Trial Master File: Gaining Efficiency for Oversight and Control
Maintaining an electronic Trial Master File (eTMF) is far more than storing study documents on the sponsor’s file server. EMA’s…
Less is the New More: Risk-based Approaches in Clinical Trials
The continuously evolving clinical research industry requires new solutions and renewed approaches. Rising costs, studies getting more and more complex…