Advance Pharmaceutical Excellence with Agentic Process Orchestration

Streamline processes, ensure compliance, and accelerate new product launches with Scheer PAS for pharma

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Why modern pharma relies on next-gen integration

The pharmaceutical industry in Germany, Austria, and Switzerland faces increasing regulatory requirements, strict quality controls, and mounting pressure to accelerate operational speed. However, disconnected IT systems, paper-based documentation, and manual handovers are hindering innovation attempts, weakening compliance, and limiting scalability. Modern pharma organisations must therefore streamline processes and tightly integrate production, labs, and quality, while at the same time automating compliance, to remain competitive and reduce time-to-market. 

Issues affecting digital pharmaceutical operations:

Manual batch processing

Fragmented documentation

Risk of regulatory breaches

Data silos in labs and plants

Inefficient supply chains

Slow product release

How Scheer PAS solves the digital factory challenge

Connected GMP workflows

Eliminate paper and unify batch records and SOPs across labs, QA, and manufacturing using seamless digital processes.

Automated compliance and documentation

Instantly generate, archive, and update documentation for GxP, GMP, and 21 CFR Part 11 securely and become audit-ready.

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Real-time process and data integration

Synchronise LIMS, MES, ERP, and supply chain data flows for true end-to-end process transparency.

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Low-code change management

Rapidly adapt workflows for new therapies, formulations, or partners, while staying within strict compliance boundaries.

Quality assurance automation

Trigger alerts, corrective actions, and deviation workflows as soon as out-of-spec data is detected.

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Secure data integrity

Built-in version control, eSignatures, and audit trails prevent data manipulation and safeguard patient safety.

How Scheer PAS connects the pharmaceutical process landscape

Ready to reimagine your processes?