Ther Innov Regul Sci. 2016 Jul;50(4):510-514. doi: 10.1177/2168479016634148.

Process Innovation Improves Trial Operation Efficiency.

Choi YJ, Kim KP, Park S, Park M, Kim S, Kim Y, Bae KS, Beck SH, Choi KE, Chung JW, Lim YS, Kim TW.

BACKGROUND:

Despite the fact that unaddressed delays in clinical trial operation could severely compromise the overall effort invested, there seems to be a lack of concerted effort in reforming such delays. This study evaluated the composite effect of initiatives in reforming trialoperation efficiency.

METHODS: A high-volume academic medical center in Korea has implemented various initiatives to improve the trial operation efficiency by expediting times from institutional review board (IRB) submission to approval, from IRB submission to trial open for subject enrollment, and from trial open to first patient-in. The initiatives include implementation of the protocol preliminary review, parallel processing of the clinicaltrial agreement review in line with the protocol submission to the IRB, and involvement of project manager for operational risk management. Times from IRB submission to approval, from IRB submission to trial open, and from trial open to first patient-in before and after implementation of initiatives were compared.

RESULTS:

The median time required in IRB approval was meaningfully shorter in the postinitiative group (19 vs 14 days; P < .001). The median times from IRB submission to trial open for subject enrollment and from trial open to first patient-in were reduced significantly in the postinitiative group (trial open: 25 vs 18 days, P < .001; first patient-in: 111.5 vs 100 days, P = .014).

CONCLUSIONS:

The initiatives were effective in reforming trial operational efficiency. Additional studies to address the cause of operationaldelay and modifiable factors influencing subject enrollment are needed to further improve operational efficiency.

KEYWORDS: clinical trial activation; clinical trial operation; clinical trial timeline; preliminary review; project manager

PMID:

30227017

DOI:

10.1177/2168479016634148