Pharmaceutical enterprises rely on structured templates, checklists, and workflows to drive production, quality assurance, R&D, and sampling. However, traditional processes remain static, paper-intensive, and resistant to change — resulting in operational bottlenecks, slowed innovation, and heightened compliance challenges. Templyn.ai addresses these issues by offering a smarter, more scalable solution to design, manage, and optimize pharmaceutical workflows.
BUSINESS NEED
Our APPROACH
With Templyn.ai, pharmaceutical organisations can:
- Self-build workflows and templates – no reliance on external teams Empower your workforce to design and adapt processes instantly, without waiting for technical rollouts.
- Standardise processes across teams and plants Ensure every site follows a consistent, structured way of working, removing variability.
- Digitalise paper-based SOPs into smart, compliant formats Convert static documents into dynamic templates that are audit-ready and always accessible.
- Automate approvals, reviews, and escalations Speed up decision-making by routing tasks automatically to the right people at the right time.
- Ensure 21 CFR Part 11 compliance Guarantee data integrity, traceability, and audit readiness with built-in compliance features.
Our RESULTS
70% faster template creation compared to traditional processes.
Improved compliance with automated approvals and traceability.
Greater efficiency by eliminating manual interventions.
Scalability across multiple plants, teams, and geographies.
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