Navigate 5 Common Pharma Challenges
Boost Efficiency and Productivity. Improve Access to Medicine.
CHALLENGE 1: Product Inconsistencies, Documentation Errors
Manufacturing Execution Systems
Enable efficient and consistent manufacturing processes
• Greater product traceability through integrated
batch genealogy and visualization
Reduce
cross-checking
hours by
Decrease
batch review deviations by
CHALLENGE 2: Complex Supply Chains, Market Disruptions
Supply Chain Planning & Scheduling
Proactively manage daily shifts in supply and demand
• Streamlined inventory management reduces holding
costs while avoiding stock outs
Reduce scheduling
time up to
compared to conventional
methods.
CHALLENGE 3: Failed Batches, Decreased Profit Margins
Advanced Process Analytical Technology (PAT)
Monitor product and process with multivariate data analysis
• Real-time release testing speeds time to market
Reduce cost of
goods sold by
for every failed batch avoided.
CHALLENGE 4: Low Equipment Reliability, High Maintenance Spend
Predictive & Prescriptive Maintenance
Use AI/ML-powered prescriptive analytics to avoid equipment downtime
• Rapid deployment and scale-out accelerate time to value
Reduce lifecycle
maintenance
costs by
Receive up to 35-day
advance warning
of impending
equipment failure.
CHALLENGE 5: Slow Commercialization of New Medicines
Process Design & Scale-up
Design for manufacturability and shorten time to market
• Shorter development timelines drive faster commercialization
and earlier access for patients
Save time on the patent clock and realize millions of dollars in revenue potential.
Read about digital’s role in minimizing the impact of supply chain disruptions.
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See how GSK and others are bringing quality medicines to patients more quickly.
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Read about the power of Advanced PAT to accelerate market growth.
See how GSK eliminated unplanned downtime to optimize its supply chain.
Read how one Japanese company developed a continuous process and improved quality.
with an Integrated Digital Strategy
• Digitally guided manufacturing execution ensures
SOPs are followed
• Electronic Batch Record compliance in accordance
with FDA 21 CFR Part 11 and EU Annex 11
• Digitally-driven planning and scheduling minimizes
waste and resource inefficiencies
• Adapting to disruptions in real time empowers staff
and enables right-first-time production schedules
Save $500K USD
• Minimizing process variability reduces waste
and bolsters quality, yield and throughput
• Reduction in batch cycle time greatly increases
operational efficiencies and improves margins
• Advance notice to production schedulers enables planned downtime
• Earlier and more accurate prediction of impending equipment failure
reduces overall maintenance costs
• Improved agility with conversion from batch to continuous
manufacturing
• Rigorous process simulation empowers Quality by Design
CHALLENGE 1:
Product Inconsistencies, Documentation Errors
CHALLENGE 2:
Complex Supply Chains,
Market Disruptions
CHALLENGE 3:
Failed Batches, Decreased Profit Margins
CHALLENGE 5:
Slow Commercialization of New Medicines
CHALLENGE 4:
Low Equipment Reliability, High Maintenance Spend
Webinar
Interview with an Expert
Solution Brief
Case Study
Case Study