Minimize waste and excess inventory with better control, shelf-life planning, and stability protocols in the supply review.
Cut expediting by approximately
30%
and unlock working capital
Genpact's implementation accelerators enable a phased, low-disruption go-live so benefits start showing fast.
Go live and de-risk change in as fast as
16
weeks and see solid value
Proactively manage clinical supply chain risks with advanced analytics – minimizing the impact on patient care and dosing.
Recover up to
10%
of revenue lost to stockouts
Fast-track clinical supplies to the sites by balancing demand and supply, adjusting to supply chain challenges as they arise.
We help companies achieve up to
30%
lower lead times – from manufacturing to availability of site-ready clinical kits
Connect your trial data and systems with IRT vendors and CMOs for inventory visibility while prioritizing security.
Streamline regulatory approvals and conquer compliance hurdles
Effortlessly manage regulatory approvals for each clinical trial by country and balance demand and supply with jurisdictional requirements and varying approval dates
Address rules for specific versions, country of origin, as well as batch-specific rules around shelf life
Use attribute-based planning designed for on-time shipments of clinical supplies to sites without regulatory bottlenecks
Master patient demand with dynamic forecasting and planning
Calculate demand curves based on study design elements, including first patient first visit (FPFV) and last patient last visit (LPLV)
Support various study designs like double-blinded, dose-escalation, and placebo-controlled trials, among others
Improve forecast accuracy and cut overages by adjusting inputs based on study design and aligning research and development activities with demand
Control drug wastage with smarter shelf-life planning
Incorporate stability protocols in the supply review process
Plan for changes in expiration dates of drugs and use stability protocols for supply selection and timing
Integrate the stability plan into the advanced planning system to help replan expiring batches and limit the number of planned orders – minimizing waste while making the right materials available when needed
Transform product life cycles with meticulous data management
Consolidate scattered, protocol-specific data that lacks integration across clinical sites and contract manufacturing organizations (CMOs)
Gain agility in life cycle management processes with supply chain master data management
Manage data with precision through years of changes as a molecule progresses through trial stages, and create a holistic supply chain network view from finished clinical goods to drug product and drug substance
Optimize clinical supply chains end to end with tailored deployment
Tackle end-to-end clinical supply planning, beyond forecasting, covering inventory, expiration tracking, distribution, and regulatory compliance
Function independently or integrate with SAP, an existing Kinaxis instance, interactive response technology (IRT), and CMOs for a unified and 100% visible supply chain
Use prebuilt templates, automation, and analytics to help deploy faster and unlock measurable benefits.
Increase speed to market with a single solution
Fully integrate supply chain planning for both your clinical and commercial supply chain practices to maximize efficiencies
Achieve greater collaboration and speed to market once approvals are secured
Maximize shared assets to support rapid profits for continued investment in research and development