An internationally recognized GxP compliance and consultancy organization delivering specialized pharmaceutical solutions across global markets
Elixir GxP Solutions is an international service organization specializing in pharmaceutical compliance and quality management solutions. The company provides GxP audits, GMP documentation support, validation & qualification, EU and PIC/S Inspection readiness and certification, eQMS/eDMS solutions, LIMS and warehouse management systems, clinical research support, regulatory consultancy, MAH services, and GMP training programs, turnkey projects, technology transfer service, warehousing services in EU, Ukraine.
Officially registered in Budapest, Hungary and London, United Kingdom, Elixir GxP Solutions supports pharmaceutical organizations globally with integrated, scalable, and internationally compliant quality solutions.
Elixir GxP Solutions having representatives in India, Africa, Ukraine & Uzbekistan.
End-to-end pharmaceutical compliance, validation, training, regulatory, and digital quality solutions tailored for global life science organizations.
Comprehensive GMP, GDP, GLP, and supply chain audits ensuring regulatory compliance and inspection readiness.
SOPs, validation protocols, quality manuals, and compliant documentation systems aligned with global standards.
Process, cleaning, utilities, equipment, and computerized system validation with lifecycle support.
Gap assessments, mock audits, remediation planning, and expert preparation for EU GMP inspections.
Gap assessments, mock audits, remediation planning, and expert preparation for PIC/S inspections.
Practical GMP and GxP training programs for pharmaceutical, biotech, warehouse, and QA teams.
Digital quality management, document control, and laboratory management software implementation and support.
Regulatory and operational support for clinical studies, documentation, compliance, and quality oversight.
Marketing authorization holding services with regulatory coordination and lifecycle management support.
GDP-compliant warehousing and distribution solutions across EU, Ukraine, and Uzbekistan regions.
End-to-end pharmaceutical facility setup, compliance planning, qualification, and operational implementation.
Structured technology transfer support ensuring process consistency, compliance, and successful scale-up.
Elixir GxP Solutions supports pharmaceutical organizations worldwide with GxP audits, validation & qualification, GMP documentation, EU and PIC/S inspection readiness, software solutions, clinical research support, regulatory consultancy, MAH services, and warehousing support across the EU and CIS regions.
Clients Worldwide Countries
Highly Qualified Auditors Globally
Audits Successfully Performed
Years of Pharmaceutical Expertise
Elixir GxP Solutions is an internationally recognized ISO 9001:2015 certified organization providing GxP auditing, validation, inspection readiness, regulatory consultancy, GMP training, eQMS/eDMS solutions, clinical support, and warehousing services across Europe, Asia, the UK, USA, and CIS regions.
Registered in Budapest and London with consultants and auditors operating globally.
Specialized support for GMP, GDP, GCP, GLP, GPvP, validation, documentation, and inspection readiness.
eQMS, eDMS, LIMS, warehouse management systems, regulatory support, and clinical research services under one platform.
A streamlined pharmaceutical compliance methodology designed to deliver efficient, inspection-ready, and globally aligned solutions.
We evaluate your existing systems, documentation, operations, and regulatory compliance status to identify gaps and improvement areas.
Our experts create a customized implementation roadmap covering compliance priorities, validation activities, training, and timelines.
We execute documentation, qualification, software systems, audits, GMP processes, and validation activities with hands-on support.
Continuous monitoring, inspection readiness, CAPA management, and ongoing quality improvements ensure long-term compliance success.
We evaluate your existing systems, documentation, operations, and regulatory compliance status to identify gaps and improvement areas.
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