Press release
GxP Cellators Announces Expansion of Regulatory Compliance and Validation Services for the Life Sciences Industry
GxP Cellators (https://www.gxpcellators.com), a leading provider of regulatory compliance, commissioning and qualification (C&Q), validation, and GxP consulting services, is proud to announce the continued expansion of its solutions tailored to support pharmaceutical, biotech, and life sciences organizations in meeting stringent regulatory standards.With a dedicated team of industry experts, GxP Cellators delivers strategic support across all phases of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) compliance, offering end-to-end services including cleanroom design qualifications, HVAC validations, equipment commissioning, and facility startup readiness.
"Companies navigating GxP compliance challenges need a partner that understands the complexity of regulatory landscapes and delivers with precision and integrity. "Our team brings decades of experience to ensure our clients achieve operational excellence while meeting FDA, EMA, and global regulatory requirements."
In addition to expanding its validation and qualification service lines, GxP Cellators continues to invest in educational content, offering free resources such as white papers, case studies, and training insights through its website blog and expert advisory sessions.
The company remains committed to empowering life sciences businesses to innovate safely and efficiently, while minimizing risk through tailored compliance strategies and quality systems implementation.
For more information about GxP Cellators and its full suite of services, visit https://www.gxpcellators.com.
David Albert
Director of Client Relations
GxP Cellators Consultants Ltd.
Email: info@gxpcellators.com
219 Baltzan Blvd, Saskatoon, Saskatchewan, Canada
We offer comprehensive Good x Practices (GxP) services in Manufacturing, Laboratory, Distribution, Engineering and Clinical practices to industries such as Biopharmaceuticals, Pharmaceuticals, and Medical Devices. Our highly qualified experts specialize in GMP, GLP, GCP, GDP, Cleanroom and Engineering operations. We provide expertise in GMP Site-readiness programs, Regulatory Affairs support, Quality Assurance/Control and Clinical Development. Our tailored services have earned us a reputation as a premier consulting entity, making us the preferred choice for enterprises seeking exceptional services.
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