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UZPHARMCONSULTING supports pharmaceutical companies with preparation for GMP, GDP, GSP, GLP, GCP, GPP and other applicable certification processes — from gap analysis and documentation to audit readiness, authority communication and full process coordination.
Explore UZPHARMCONSULTINGManufacturing quality systems and production compliance preparation
Distribution, warehouse and storage practice preparation
Laboratory and clinical practice documentation support
Pharmacy practice and retail compliance preparation
UZPHARMCONSULTING provides structured certification support for pharmaceutical companies, manufacturers, distributors, warehouses, laboratories, pharmacies and other healthcare-related organizations.
The company supports preparation for GMP, GDP, GSP, GLP, GCP, GPP and other applicable standards by reviewing existing processes, identifying documentation gaps, preparing internal procedures, supporting audit readiness and coordinating communication throughout the certification pathway.
Our role is to help partners build a clear, controlled and documented system before certification, inspection or expert review.
GxP certification and inspection processes in Uzbekistan are connected with the applicable pharmaceutical legislation and regulatory requirements of the Republic of Uzbekistan, including Resolution of the Cabinet of Ministers No. 788 of September 18, 2019, related to the introduction of Good Practice (GxP) requirements in the pharmaceutical sector.
The introduction of Good Practices in the pharmaceutical sector, including GMP, GDP, GLP, GCP, GSP and related standards, is supported by the regulatory framework established for pharmaceutical quality systems and inspections, including activities coordinated through the Center for Good Practices, which maintains registers of issued certificates across GMP, GDP, GLP, GCP, GSP and GPP areas.
UZPHARMCONSULTING supports partners in preparing documentation, quality systems, procedures and audit-readiness materials in line with applicable requirements.
Information on this page is provided for general business purposes and does not replace official review by competent authorities or certification bodies. Certification outcomes depend on the organization's actual processes, documentation, facility readiness, expert review and applicable regulatory requirements.
UZPHARMCONSULTING supports preparation for key pharmaceutical Good Practice standards and related certification pathways.
Good Manufacturing Practice
Preparation for manufacturing quality systems, production documentation, SOPs, personnel training, quality management processes and audit-readiness requirements.
Good Distribution Practice
Support for distribution systems, warehouse operations, logistics processes, temperature control, documentation, traceability and responsible pharmaceutical supply.
Good Storage Practice
Preparation of storage conditions, warehouse zoning, product handling procedures, temperature monitoring, documentation and storage compliance systems.
Good Laboratory Practice
Support for laboratory documentation, quality systems, testing procedures, records, data integrity and laboratory process readiness.
Good Clinical Practice
Documentation and process support related to clinical research standards, study documentation, ethics-related coordination and clinical practice requirements where applicable.
Good Pharmacy Practice
Support for pharmacy practice standards, retail pharmacy processes, documentation, responsible dispensing environment and quality-related preparation.
Support for additional quality, regulatory and certification-related requirements depending on product type, activity model and business process.
UZPHARMCONSULTING provides end-to-end certification preparation support.
The process may include initial assessment, gap analysis, documentation development, SOP preparation, quality system review, personnel training coordination, audit-readiness preparation, internal pre-audit, corrective action planning and communication with relevant authorities or certification bodies.
Certification is not only a document submission process. It requires a working system that can be reviewed, inspected and verified.
UZPHARMCONSULTING helps partners prepare for audits and inspections by reviewing documentation, checking process logic, identifying risks, supporting staff preparation and organizing corrective actions before formal review.
GxP certification requires structured preparation, documentation discipline, process control and understanding of applicable pharmaceutical requirements.
UZPHARMCONSULTING provides a practical certification pathway for companies that need to prepare their operations, documentation, personnel and quality systems for inspection or certification.
End-to-end support from initial assessment to certification follow-up
Structured preparation of SOPs, QMS documents, records and audit materials
Preparation of processes, staff and documents before inspection or expert review
Communication and follow-up support with relevant authorities and certification stakeholders
Companies may submit information about their activity, facility, documents and certification goals for initial assessment by UZPHARMCONSULTING.
The review may include applicable GxP standard, current documentation status, facility readiness, process gaps, audit-readiness needs and possible next steps.
If confidential information is exchanged, UZPHARMCONSULTING or MEDTRADE may request or offer a separate Non-Disclosure Agreement.
UZPHARMCONSULTING supports pharmaceutical companies with turnkey preparation for GMP, GDP, GSP, GLP, GCP, GPP and other applicable certification processes — including documentation, audit readiness, quality system support, authority communication and process coordination.
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