We Build Workflow Software Specifically for Pharmaceutical Operations.
SQUETIKA is an early-stage software company. We are not a large enterprise vendor, and we do not sell generic compliance platforms. We work with pharmaceutical teams to understand their specific workflows and build digital systems that reflect them — accurately, practically, and in compliance with the regulations that govern the industry.
Built because we kept seeing the same problems.
The team behind SQUETIKA has worked closely with pharmaceutical manufacturing and quality operations. Across different facilities and different organisations, we kept seeing the same recurring problems: paper batch records with missing entries, CAPA trackers in spreadsheets that nobody updated consistently, SOPs stored in shared drives with no version control, e-signatures that were nothing more than a typed name.
The generic software options that existed were either too expensive and complex for mid-size manufacturers, or too rigid to fit the way teams actually operated. Both paths required the organisation to change its processes to fit the software.
We started SQUETIKA to build the alternative: software that starts from your existing processes and maps them into a digital system — not the other way around.
We are early-stage and we're honest about it.
We don't have a decade of enterprise implementations to point to. What we have is deep understanding of pharmaceutical workflow challenges, a focused approach to solving them, and the ability to move quickly because we are a small, specialist team.
If you choose to work with us, you work directly with the people building the system — not with an account manager who doesn't know the product.
Our focus is narrow by design.
We only work in pharmaceutical and life sciences. This isn't a general software firm that happens to have a pharma product line. Every tool we build, every team member we bring in, every design decision we make is shaped by the specific requirements of this industry.
Our operating principles.
Process First, Software Second
We do not start a project by showing you a product. We start by understanding your workflows — your SOPs, your approval chains, your data requirements, your regulatory context. The software is built from that understanding.
Compliance Is Designed In, Not Bolted On
21 CFR Part 11, ALCOA+ data integrity principles, and GAMP 5 validation guidance are not features we add at the end of a project. They are the framework within which every design decision is made — from how audit trails are stored to how e-signatures are implemented.
We Stay Involved After Go-Live
Systems reveal their real-world complexity once people start using them. We treat post-implementation support as part of the project, not as an add-on service. Our relationship with clients typically deepens after the initial system goes live.
We Tell You When We're Not the Right Fit
If a client's requirements would be better served by a large enterprise platform, or by a solution we are not positioned to build well, we say so. Our reputation is built on solving the right problem, not on closing every sale.
Architecture
Modules
Framework
No Generics
Our core solution areas for pharmaceutical teams.
Quality Management (QMS)
Deviations, CAPAs, and change control built for 21 CFR compliance.
Document Control
Version-controlled SOPs and protocols with automated review cycles.
Electronic Batch Records (eBMR)
Real-time data capture on the shop floor with step-by-step validation.
Electronic Signatures
Manifestation of intent with full identity verification and audit trails.
GMP Manufacturing
Facility-specific modules for equipment logs, environmental monitoring, and inventory.
Clinical Research Tools
Data capture and trial management systems built for high integrity.
Ready to talk about your specific workflow?
Every engagement starts with a conversation about your process. No demos of pre-built software — just an honest discussion about what you need and whether we can build it.