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Management of clinical supplies in clinical trials has become a major hurdle in this new era of clinical research. With the complex challenges that clinical trials shoot in terms of the design or the study population or the subgroup categorization has put the supply chain managers in a critical pose.<br><br>IRT shall ease the work of the Supply Chain Managers by taking prior measures of a few main factors that hamper the management of the clinical supplies at sites. The new designs in the clinical study conduction involve the multi-centers that are in National and International locality.
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BLOG Measures to Overcome Low Stock Supplies in Clinical Trials Using IRT Management of clinical supplies in clinical trials has become a major hurdle in this new era of clinical research. With the complex challenges that clinical trials shoot in terms of the design or the study population or the subgroup categorization has put the supply chain managers in a critical pose. IRT shall ease the work of the Supply Chain Managers by taking prior measures of a few main factors that hamper the management of the clinical supplies at sites. The new designs in the clinical study conduction involve the multi-centers that are in National and International locality. A few of the main factors to be considered to take appropriate measures are: Maintaining an adequate quantity of supplies at site by the time the site is activated and the enrollment process is initiated. ? Taking appropriate measures to ship the supplies to multi-sites located nationally & internationally. ? Maintaining and shipping the supplies that are safe and not meeting the expiry in near future. ? Shipping the supplies by meeting the regulatory guidelines and standards. ? Read More www.DDIsmart.com