In the ever-evolving pharmaceutical industry, designing and setting up compliant, efficient, and scalable facilities is critical to meeting regulatory requirements and ensuring product quality. Whether it’s a Greenfield project starting from scratch or a Brownfield project optimizing existing facilities, Qualifyo brings unmatched expertise to guide your organization through the entire process. With our specialized approach, we ensure that your facility aligns with global standards like WHO, PIC/s, EU GMP, and USFDA, making your operations future-ready.
At Qualifyo, we adopt a structured, end-to-end approach for facility design and setup:
Detailed layouts for manufacturing, quality control, warehousing, and utilities that meet GMP requirements.
Guidance to ensure facility construction and equipment setup aligns with applicable standards.
Address potential non-compliance risks during facility setup.
Facility designs that accommodate future expansions or upgrades seamlessly
With over 20 years of experience and collaborations with experts worldwide, we bring unparalleled regulatory knowledge.
Tailored audit frameworks for each client, ensuring precision and relevance.
Trusted by pharmaceutical giants across continents.
From planning to post-audit corrective actions, we’re with you at every step.
Speak with our experts to explore tailored solutions for your project.
Share your project details to receive a tailored proposal and cost estimate.
Speak to Our Experts at +91 9898573080
If you have a General enquiry, please drop me an email
Email: bd@qualifyo.com
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