I nostri servizi
Manufacturing
Our facility has an area dedicated to manufacturing activities, able to provide manufacturing services, in accordance with the EU-GMP / CGMP.
Packaging
Drugs Primary and secondary packaging for experimental clinical use are the core activity of the Euromed Pharma Services pharmaceutical facility.
Labeling
A large area of the facility is dedicated to the packaging and labeling for investigational drugs
Comparator Sourcing
Network of partner suppliers for sourcing products from the international market
Import from third countries
QA Unit and Logistic Unit able to manage the import and release of material from third countries
Narcotics management
Possibility of packaging and distribution of narcotic drugs for experimental clinical use
Destruction
Sponsor support service for the management of the final part of the clinical trial life cycle
Return and Reconciliation
Management and reporting of withdrawal service for Clinical Trial expired and not expired drug, reconciliation and storage
Storage
A warehouse dedicated exclusively to the Clinical Trial for storage according to GMP standards.
Management of stocks and movements through a dedicated ERP system
Commercial drug
The pharmaceutical facility is able to provide packaging services on commercial drugs
Distribution
Competence, high responsiveness, flexibility and a wide range of options for the distribution of IMPs in Italy, in Europe and all around the world.
Analytical Support
Laboratory and staff dedicated to stability studies, analysis and quality control
Other services
The widespread knowledge of IMP management allows us to provide numerous additional services
FAQ Clinical Trial
To start a collaboration with us, you can contact us through our online contact form or send us an email. We will guide you through the entire process, from trial design to distribution, ensuring that all regulations are met.
Euromed Pharma Services operates in accordance with Good Manufacturing Practices (GMP), ensuring that all our manufacturing, packaging and labeling processes are performed according to international standards. Our production area is inspected regularly to ensure the highest quality and regulatory compliance.
Pharmaceutical logistics is a key aspect in clinical trials. We handle the distribution of products to research sites, the management of returns, and the storage of drugs in optimal conditions to ensure their efficacy and safety. In addition, we offer destruction services for unusable or expired drugs.
You can send us a detailed request via our online contact form or by email. We will ask you to provide us with specific information about the products needed, quantities required, and timelines. Our team will work to identify the most suitable suppliers and ensure timely delivery to you.
Yes, Euromed Pharma Services offers packaging customization services for your products. We can tailor packaging to your specific needs, including sizes, designs and materials. Whether it's single-serve packaging, custom boxes, or multilingual labels, we work with you to create packaging that complies with local regulations and meets your compliance and distribution needs.
We offer extensive quality support at all stages of the product life cycle, from production to distribution. We deal with:
- Quality control;
- Quality assurance;
- Laboratory analysis and testing;
- Verification of regulatory compliance;
- Documentary and regulatory management to ensure that products comply with international standards and regulations.
Yes, Euromed Pharma Services supports clinical trials both nationally and internationally ensuring compliance with local and international regulations. Euromed Pharma services manages the entire process of planning, manufacturing, verification and distribution of the necessary products, assisting in the preparation of quality documentation and logistics.
