Batch release testing
GMP Certification and Market Release of Medicinal Products Imported from Third Countries
UAB Eletis Medica provides professional medicinal product certification and market release services in compliance with Good Manufacturing Practice (GMP) requirements. Our goal is to ensure that every batch of medicinal products supplied to the European Union market meets all applicable quality, safety, and regulatory standards.
Our team consists of qualified specialists responsible for the quality evaluation and certification of medicinal products in accordance with European Commission directives and European Medicines Agency (EMA) guidelines. All procedures are carried out in line with current GMP standards, ensuring that products manufactured both within the European Union and in third countries are approved by a certified Qualified Person (QP).
Our services cover the full batch evaluation cycle:
- Receipt and storage of medicinal products
- Sampling and laboratory testing
- Qualitative and quantitative analysis according to validated methods
- Batch certification of medicinal products
- Market release of medicinal products following successful evaluation
UAB Eletis Medica also provides certification services for medicinal products imported from third countries. We perform all necessary inspections, documentation reviews, compliance assessments, and release authorizations in accordance with European Union GMP requirements. Our processes ensure that every product released to the market is reliable, safe, and meets the required quality standards.
Certification is performed by a Qualified Person (QP) authorized to release medicinal products to the European market. This service enables manufacturers and distributors to efficiently and promptly place products on the market while maintaining full regulatory compliance.