SERVING HEALTHCARE FACILITIES

Farmaceutica Internazionale Italiana

TOGETHER since 2008 WE FACILITATE ACCESS TO NEXT-GENERATION AND HARD-TO-SOURCE MEDICINES We support hospitals and clinics in the responsible procurement of unlicensed, short-supply or limited-availability medicines, with a particular focus on quality and professional ethics
Since 2008

Serving healthcare

Founded in 2008, our company operates as an international pharmaceutical wholesaler supporting public and private healthcare facilities.

We assist hospitals and clinics in managing hard-to-find, unregistered in Italy, and/or in short supply medications, offering a complete service that combines regulatory expertise, quality control and a consolidated network of validated and selected international partners.

Each supply is managed with care, transparency, and full compliance with current regulations, to ensure safety for healthcare professionals and patients.

1. Proven experience
Over 15 years of experience in the international pharmaceutical sector, working alongside public and private healthcare facilities.
2. Partners, not mere suppliers
We collaborate with over 300 qualified suppliers in more than 20 countries, building relationships based on reliability and continuity.
3. Uncompromising quality and compliance
We operate according to ISO 9001 and GDP standards and supply only medicines with valid and verified GMP certification.
4. Full and responsible management
We follow every step: from the request, to the documentation required by local authorities, up to delivery, ensuring traceability and control.
A complex, regulated, and constantly evolving market

The context in which we operate

International access to medicines is characterized by increasing complexity today. The significant increase in drug shortages, the constant search for medicines not registered in Italy, and the continuous evolution of regulations make procurement a process that requires specific skills, attention, responsibility, and above all, EXPERIENCE.
MEDICINE SHORTAGES A rapidly growing global phenomenon that continually challenges healthcare facilities, forcing them to engage with foreign markets to ensure therapeutic continuity for patients.

Differentiated authorization procedures

Stay on top of your projects with detailed analytics and progress tracking. Visualize performance, monitor key statistics, and measure milestones effortlessly.

Unforeseeable logistical variables

Customs controls, anti-counterfeiting procedures, and transport-related delays can affect procurement times and require careful and conscious management: our streamlined model covers every stage of logistics, ensuring speed and maximum reliability in deliveries

Responsibility in operational choices

In such a complex context, we always prioritize quality, compliance, and safety over seemingly faster solutions that lack the necessary guarantees.
WHAT WE DO

When do we intervene?

We support public and private healthcare facilities in managing critical pharmaceutical supply situations, unregistered and/or scarce medicines, offering solutions compliant with current regulations and comprehensive support at every stage of the process.

Unlicensed Medicines

We manage the supply of medicines regularly authorized abroad but not registered in Italy, supporting healthcare facilities in preparing the required documentation and complying with AIFA and USMAF procedures.

Drug shortages

We intervene in cases of temporary shortage or unavailability on the Italian market by activating our network of international suppliers to ensure therapeutic continuity, subject to production and distribution availability.

Our international network

300+

Active qualified suppliers

Partners selected and verified according to quality and compliance criteria
20+

Sourcing countries

International network in Europe and non-EU countries
100%

GMP-compliant supplies

Only medicines with valid and verified GMP certification
18+

Years of experience

Ongoing activity since 2008
RECOGNIZED STANDARDS AND VERIFIABLE PROCESSES

Certified quality system

Certifications and awards to support verifiable and compliant processes.

Our goal is to consistently exceed our customers' expectations.

GDP – Good Distribution Practices

Certification confirming the proper management of medicinal product distribution, in compliance with good practices throughout the entire supply chain.

IQNet – Recognized Certification

International recognition that confirms the validity of ISO certifications issued by accredited bodies, ensuring their global value.

ISO 9001

Certification of the quality management system, which guarantees structured, traceable processes geared towards continuous improvement.


OPERATIONAL CONTROL AND COMPLIANCE

Quality and compliance

We operate according to rigorous quality standards and regulatory compliance, aware of the responsibility that each pharmaceutical supply entails for healthcare facilities and patients. Our management system is ISO 9001 certified and ensures structured, traceable, and constantly monitored processes at every stage of activity. The distribution of medicines takes place in compliance with Good Distribution Practices (GDP), ensuring proper management of the supply chain, from collection to delivery. We exclusively supply medicines produced in facilities compliant with Good Manufacturing Practices (GMP). Each lot is subject to control by the Quality department, with verification of certifications' validity and the correspondence of the data reported on the packaging, guaranteeing safety, transparency, and full compliance with current regulations.
Regulatory compliance guides every operational decision.
FROM REQUEST TO DELIVERY

How do we work?

We manage every supply through a clear and controlled process, designed to ensure regulatory compliance, drug quality, and comprehensive support to healthcare facilities at every stage.
1

Request analysis

We evaluate each specific case and the regulatory context, defining the most suitable procedure based on the type of drug and clinical urgency.

2

Regulatory and document management

We support the healthcare facility in preparing the necessary documentation and fulfilling the requirements requested by the competent authorities.

3

Procurement and Quality Control

We activate our network of qualified international suppliers and verify drug compliance, including the validity of GMP certification.

4

Logistics, Delivery and Support

We manage transportation and customs procedures, ensuring traceability right up to delivery. We guarantee continuous customer support, backed by our scientific staff.

Our guarantees

Reliability and control at every stage of the supply chain

Regulatory compliance

Every supply is managed in compliance with current regulations and the procedures applicable to each individual case.

Quality control

All medicines undergo rigorous quality controls: our QA (Quality Assurance) ensures compliance with the standards required by the reference regulations.

Full traceability

Every stage of the process is documented and traceable, from the initial request to delivery.

Ongoing support

We support healthcare facilities with constant operational and regulatory services at every stage, from tendering to supply, ensuring continuous and highly specialized assistance.

possiamo aiutarti?

Contatta il nostro Team

Il nostro Team è a disposizione per supporto operativo, gestione degli ordini, richieste di offerta e/o chiarimenti normativi.

Ufficio Commerciale

commerciale@finternazionale.it commerciale2@finternazionale.it

Ufficio Ordini

ufficio.ordini@finternazionale.it elena.filippetti@finternazionale.it

Amministrazione

amministrazione@finternazionale.it amministrazione2@finternazionale.it

Ufficio Import

ufficio.clienti@finternazionale.it ufficio.clienti2@finternazionale.it

Ufficio Legale

support@finternazionale.it

Qualità e Regolatorio

direzionetecnica@finternazionale.it

Contact us

Request for information or offer

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OPERATIONAL GUIDELINES

FAQ

For unregistered drugs, you must receive the declaration of responsibility completed in all missing parts, stamped and signed by both the prescribing physician and the pharmacy department.

We will take care of sending the documentation to the USMAF offices for the release of the health clearance.

For drug shortages, the healthcare facility must send the completed documentation, with the missing sections filled in, stamped, and signed as required, directly to AIFA at the email address provided in the form.

AIFA will issue the authorization directly, which must then be subsequently sent along with the order.

To request a quote, you can contact our sales office by phone or email.


Phone


+39 0323 86 55 57


Email

Following your request, we will be pleased to send our best offer together with supporting documentation, which may include:

  • Original drug data sheet
  • Pre-filled liability waiver (for drugs not registered in Italy)
  • Pre-filled AIFA form (for drugs with temporary shortages)