Wonderful experience!
Their thorough GMP supplier audits helped us identify critical areas for improvement, ensuring full compliance with regulatory standards. We were impressed by their attention to detail and commitment to quality assurance.
Pharmaceutical organizations operate in a highly regulated environment where compliance with standards like WHO, PIC/s, EU GMP, and USFDA is not optional—it’s critical. Certification and accreditation validate a company’s commitment to quality, safety, and regulatory compliance, ensuring market access and customer trust. At Qualifyo, we bring decades of GxP expertise to help organizations achieve these essential certifications seamlessly.
In today’s competitive pharmaceutical landscape, adhering to global standards is essential for:
Ensures compliance with international regulations to avoid costly delays or penalties.
Facilitates entry into regulated markets globally.
Facilitates entry into regulated markets globally.
Obtaining certifications like WHO, PIC/s, EU GMP, and USFDA demonstrates your commitment to quality and builds confidence among stakeholders.
Comprehensive Compliance Roadmaps tailored to your organization’s needs
Fully documented Quality Management Systems (QMS) that align with certification standards
Ready-for-inspection facilities and systems.
Successful certification or accreditation outcomes.
Over 20 years of global GxP and regulatory compliance experience
: Custom strategies aligned with your operational goals.
In-depth knowledge of international regulatory requirements
A history of successful certifications for leading pharmaceutical organizations
Partner with Qualifyo to streamline your certification journey and secure your place in global pharmaceutical markets.
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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