How Euromed Pharma optimizes study launch efficiency
Uninterrupted clinical supply chain management: the Euromed Pharma assurance
The increasing complexity of trial design implies a significant number of variables to bring a molecule to its development and commercialization.
We put together a service offering that reduces the risk of delays in the supply chain, by assisting the client since the early stage of protocol drafting throughout the whole duration of the study.
We can advise our clients on the best procurement strategy and put in place a back-up plan in case of shortages, to avoid any stock-outs during the trial.
This is feasible thanks to our physical presence in 10 countries, with direct access to manufacturers in all of them and a network of qualified wholesaler partners in more than 50 countries, established in over 60 years of activity.
Our broad network assures short delivery timelines, guaranteeing that the medications are on site when and how planned.
A comprehensive support to the Pharmaceutical and Biotechnology Industry
Ensuring steady supply for patient success in clinical trials
Euromed Pharma Services can support the Sponsors throughout the entire execution of their trials:
Clinical Supply Consulting
- Suggesting the best Packaging/Labeling solutions
- Strategical approach to Drug Procurement since the early stages of the Protocol Definition
- Comparator and Ancillary Sourcing
- Sourcing IMPs, AMPs, Concomitant, Background and Rescue Medications
- Import and Export from and to EU.
- A team dedicated only to Ancillary and Medical Device procurement
Clinical manufacturing – EU based (Clinical Manufacturing, Packaging, Labelling) & Management of Investigational Medicinal Products (IMP):
MANUFACTURING
- Blinding of IMP – e.g., over-encapsulation of a solid oral formulation
- Placebo capsules manufacturing to match IMP under evaluation
- Batch release and certification by QP (QP release services)
PACKAGING
- Primary Packaging of oral solid formulations
- Packaging of all formulations and high potency drugs in cooperation with qualified partners
- Secondary packaging of all formulations and packaging designs at our production sites
- Provision of user-friendly packaging materials, controlled to fit quality specifications
LABELING
- Preparation of label text according to regulatory requirements
- Label design to enhance compliance of trial subjects
Direct access to pharmaceuticals and ancillaries through Euromed Pharma
A 360° approach to pharmaceutical and ancillary sourcing
- Strategic planning – market accessibility intelligence
- Assistance in Protocol Development for early feasibility studies
- A full-line wholesale approach to clinical supply challenges
- Prescription drugs
- Hospital lines
- Over the counter (OTC) medicines,
- Medical and surgical devices
- Ancillaries
- Direct access to major pharmaceutical manufacturers where we have our own affiliates
- Licensed wholesalers and warehouses in 7 EU countries + USA and Singapore
- Access to Product Documents, such as Certificate of Analysies (CoA), Certificate of Conformity (CoC) and Certificate of Origin (CoO)
- Import/Export and Custom Clearance services
Together throughout your drug’s lifecycle
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