Tomorrow’s therapies demand a flexible solution today.
Pharmaceutical manufacturing faces constant challenges
Waste and scrap are high, and unexpected issues deter full capacity utilization and schedule adherence. Siloed data and largely paper-based systems prevent required process visibility for increased quality and operational improvements. Existing systems are too rigid to accommodate increasing fluctuations in demand and the introduction of new drugs. At the same time quality and compliance are paramount, but they are costly and burdensome with existing approaches.
Existing systems are too rigid
Quality and compliance are burdensome
High cost of waste & scrap
Lack of visibility due to siloed data
Tulip’s no-code platform reduces cost of quality while making compliance seamless.
Tulip apps can help simplify instructions for complex processes, bring quality in-line, and enforce regulatory compliance. Electronic signatures, audit logs, and automatic data collection ensure data integrity and traceability. And its flexibility allows manufacturers to respond quickly to fluctuations in demand.
Make seamless compliance an inherent part of your digital transformation.
Audit logs and a digital approval process ensure 100% traceability into activity.
80% Reduction in Line Clearance Process Time within 4 Weeks
A leading pharmaceutical manufacturer reduced a 10-day line clearance process to 2 days using a centralized shop floor app built on Tulip.