Regulatory V7 I4 Archives - Journal for Clinical Studies

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Editorial Archive

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 initiative has enjoye...

20 August 2015 Editorial Archive | Regulatory V7 I4 | Volume 7 Issue 4

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Editorial Archive

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 reflection paper on Trial Master Fil...

20 August 2015 Editorial Archive | Regulatory V7 I4 | Volume 7 Issue 4

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Editorial Archive

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 and, what is...

20 August 2015 Editorial Archive | Regulatory V7 I4 | Volume 7 Issue 4

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Journal for Clinical Studies

Journal For Clinical Studies has a distinguished editorial advisory board providing the best guidelines for global clinical trials. Your resource for Multisite Studies and emerging markets.

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Vaccine – Shorten Start-Up Timelines in Vaccine Trials

Current Edition

Converge or Be Purged: IDMP Product Standardisation Deadline Looms

Electronic Trial Master File: Gaining Efficiency for Oversight and Control

Less is the New More: Risk-based Approaches in Clinical Trials

Journal for Clinical Studies