Let's Talk About Your Workflow.
We don't start with a product demo. We start by understanding your specific process — what you're doing today, where it's creating friction, and what a better system would need to do. Fill in the form or email us directly. We'll respond within one business day.
We Read Your Message
We review every inquiry personally. If you describe a specific workflow challenge, we'll come prepared with relevant context — not a generic sales deck.
We Schedule a Call
A 30–45 minute conversation to understand your process, your team structure, and where the real pain points are. We listen more than we talk in this meeting.
We Share a Proposed Approach
Based on what we learn, we'll outline how a system could work for your specific situation — what it would include, what it wouldn't, and what a realistic timeline looks like.
You Decide
No pressure, no automatic follow-up cadence. If the approach makes sense for your organisation, we move forward. If not, we'll tell you what we think would serve you better.
We'll review your message and respond within one business day. If your situation is urgent, email us directly at squetikatechnology@gmail.com.
Things people usually ask before reaching out.
Do you work with small pharmaceutical companies or only larger manufacturers?
We work with pharmaceutical companies of various sizes, but we are particularly well-suited to mid-size and growing manufacturers who need structured digital systems but don't have the budget or appetite for large enterprise platforms. The size of the organisation matters less to us than the specificity of the problem.
How long does implementation typically take?
It depends on the scope and complexity of what we're building. A focused module — like a CAPA workflow or document control system — can typically be implemented in 6–12 weeks. Larger projects with multiple interconnected modules take longer. We give honest timelines from the start, not optimistic estimates that slip.
Is the software validated for 21 CFR Part 11 compliance?
Our systems are designed with 21 CFR Part 11 requirements as a baseline — audit trails, e-signature mechanics, access controls, and record integrity. We provide documentation to support your validation effort (IQ/OQ protocols), but formal validation is a client-side activity. We'll walk you through what we provide and what your team needs to do.
We already have an ERP or QMS — can you integrate with it?
This is something we discuss during the initial consultation. Integration capability depends on the systems involved and what APIs they expose. We've built connectors to common platforms, and we're transparent about what's feasible within a given scope and budget. We won't promise integrations we can't deliver.
What does it cost?
We don't publish standard pricing because every project is configured differently. After understanding your requirements, we provide a fixed-scope proposal with clear pricing. There are no hidden fees or surprise add-ons. If our quote is outside your budget, we'll tell you what a reduced scope could look like.