About Us
Our Story
Ecovita began with a clear purpose: to bridge the gap between pharmaceutical innovation and regulatory excellence. Founded by industry professionals with over a decade of hands-on experience, our journey started with a simple yet powerful idea — to support pharmaceutical companies in building efficient, compliant, and future-ready systems from the ground up.
In our early days, we observed that many pharma businesses, especially startups and mid-sized firms, struggled with ever-evolving compliance standards, complex facility requirements, and the pressure of audit readiness. That’s when Ecovita stepped in — not just as a consultancy, but as a partner in progress.
- Decade-Strong Expertise
- Regulatory Mastery
- Customized, Practical Solutions
- From Vision to Validation
What We Offer
we deliver end-to-end pharmaceutical consultancy solutions designed to ensure operational excellence, regulatory compliance, and sustainable growth. Whether you’re launching a new facility or streamlining an existing one — we provide the expertise, tools, and strategy to help you succeed.
We Understand Requirements
We listen, analyze, and understand your unique needs before we act. Every pharmaceutical facility, process, and team has its own challenges — and we make it our priority to understand them from the ground up. With over a decade of hands-on experience, we’re able to anticipate regulatory expectations, spot operational gaps, and offer tailored solutions that work in real-world scenarios. We understand pharma processes inside out, ensuring designs that work in practice, not just on paper.— we align our strategies with your goals, your timelines, and your vision.
We Work Precisely
Precision isn’t just a value — it’s our way of working. In an industry where even the smallest detail can impact quality, compliance, and safety, we bring unmatched attention to detail in every step of the process. From designing plant layouts to drafting SOPs, from equipment qualification to audit preparation — accuracy and compliance drive our every action. We combine regulatory knowledge with technical expertise to ensure that every plan, document, and system we deliver is aligned with global standards and tailored to your facility. Because in pharma, precision isn’t optional — it’s everything. And at Ecovita, we make it our promise.
Compliance-Focused Solutions
In the pharmaceutical industry, compliance is non-negotiable — and at Ecovita, it’s at the core of everything we do. We specialize in designing solutions that not only meet today’s regulatory standards but also anticipate tomorrow’s requirements. Whether you're preparing for a WHO-GMP, USFDA, EU-GMP, or CDSCO inspection, we ensure your facility, documentation, and processes are fully aligned and audit-ready. With our structured, risk-based approach, we help you build systems that are efficient, scalable, and built to pass every inspection — the first time. We don’t just help you pass audits — we help you build a culture of compliance that sets you apart in the market.
Our Expert Team
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We believe every Pharmaceutical unit has the potential to be world-class
And, We’re here to help you make it happen.