DRUG AND DEVICE LOGISTICS

Mitigate risk and create closer connections throughout the patient journey.

EASE THE BURDEN

COVERING END-TO-END CLINICAL TRIAL SUPPLY MANAGEMENT LOGISTICS.

Our suite of solutions provide the flexibility to handle medical device or drug logistics . Both logistic workflows are connected through our EDC (Electronic Data Capture) and RTSM (Research Trial Supply Management) systems. We’ve tailored our offerings specifically to address the client needs for these kind of studies.

USE CASE FEATURES

MEDICAL DEVICE LOGISTICS
  • Returns/Reship
  • Quarantine workflows
DRUG LOGISTICS
  • Expiry dates management
  • Automatic resupply
  • Code break workflow functionality including wrongly dispensed drugs

BENEFITS

Depot and Store Management

Keeping track of inventory at the depot and stores consisting of kit code list update, stock issue and returns, quarantine, indent approvals and blocking kits.

Stock issue, Receipt, Transfer and Returns

Comprehensive Inventory management consisting of the stock issue to sites, receipt by sites, transfer and returns from sites and logistics tracking during issue/transfer.

Emergency Unblinding

Randomisation team can unblind individual patient treatment protocol following an unblinding process.

Auto / Manual Indents

Auto indents generation based on-site Inventory reorder level or raise manual indents. Both have to follow the stock approval workflow for stock issues by the depot.

Allotment

Drug or device allotment to patients in EDC based on the treatment arm assigned during randomisation.

Returns / Reship

Device return and re-allotment to patients. Add to inventory or quarantine.

Supply Management

Comprehensive Supply Management schemes (buffer & predictive) w/ability to alter plans in real-time throughout the study. Utilize pooling to save on inventory.

Robust Cohort Management

Powerful features that support adaptive trials and ability to make mid-study changes to treatments and visit schedules with limited to no downtime. Be able to move patients between cohorts.

Kit Code List Management

Upload Kit Code List to the central depot to manage IP inventory for the study. Define kit allocation and treatment arm for kits.

MRL Upload

Upload the Master Randomisation List (MRL) to manage subject randomisation and treatment arms across the study and various sites. Manage block and stratified randomisation using the MRL.

RESOURCES

Meet EVIDENTIQ at the ACDM in Edinburgh

The Association for Clinical Data Management (ACDM) Annual Conference has been running for over 30 years. It is just 3 weeks to go until delegates, ...

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Decoding the alphabet soup: a guide to clinical research acronyms

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Scope summit for clinical ops executives, orlando florida feb.7-10

Are you going to the SCOPE Summit for Clinical Ops Executives? So are we. Step by our booth ...

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Meet EVIDENTIQ at the ACDM in Edinburgh

The Association for Clinical Data Management (ACDM) Annual Conference has been running for over 30 ...

Learn More

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