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We Are Specialists in Comparator / RLDs and Clinical Trial Ancillaries

At Pro Pharmaceuticals Group, we specialise in the precise sourcing and procurement of commercial pharmaceuticals tailored to meet the specific demands of clinical trials. As we continually strive to enhance our global operations, we are exploring opportunities to expand our services in Europe to better serve our clients worldwide.

Our Expertise in Comparator and RLD Sourcing

Pro Pharmaceuticals Group excels in the precise sourcing of pharmaceuticals for clinical research.

 

By forging strategic partnerships with CROs, CDMOs, and multinational clients, we ensure seamless procurement and distribution of comparators and RLDs. Our process, supported by a robust global network of suppliers, adheres to stringent SOPs for every step, from procurement to transport and customs clearance

— all to deliver unmatched client satisfaction and continuity in the supply chain.

PARTNER WITH US, GET IN TOUCH

ProPG Biological RLD Sourcing

Our Pledge to Excellence: Quality and Compliance at Pro Pharmaceuticals Group

At Pro Pharmaceuticals Group, we are dedicated to delivering the highest quality pharmaceutical solutions with an unwavering focus on compliance and operational excellence. Our licensed facilities in Melbourne, Australia; Hamburg, Germany; and Warsaw, Poland enable us to provide seamless services globally, catering to the diverse needs of clinical trials, research organizations, and healthcare providers.

With a strong foundation in regulatory standards, advanced infrastructure, and strategic partnerships, we are uniquely positioned to ensure the integrity and safety of every product we handle.

Australia: Quality and Compliance

Our Melbourne facilities adhere to the stringent standards of Australian Good Distribution Practice (GDP) and ISO 9001 accreditation. Featuring advanced temperature-controlled systems, they guarantee the integrity and safety of every product throughout the supply chain.

As a licensed wholesaler, we uphold the highest standards of regulatory compliance and operational excellence, delivering reliable services for clients across the Asia-Pacific region and beyond.

Germany: Global Reach and Standards

Located in Hamburg, our German facilities are accredited under EU Good Distribution Practice (EU GDP) and ISO 9001:2015. These state-of-the-art facilities enhance our ability to serve the European Union and international markets.

 

By maintaining the same rigorous quality and compliance standards as our Melbourne facilities, our Hamburg site strengthens global operations, ensuring efficient, reliable, and secure pharmaceutical distribution.

 

Poland: Specialized Services

Partnering with an EU-GMP certified manufacturing site in Warsaw, we offer specialized services including secondary labeling and Qualified Person (QP) release for pharmaceutical products. These services ensure compliance with EU regulatory requirements.

 

This collaboration enables us to meet the critical needs of clinical trials and research organizations globally, reinforcing our position as a trusted partner for pharmaceutical solutions.

Core expertise 

  • Prix compétitifs et niveaux élevés de  Service client 

  • Expérience et expertise depuis 2015

  • Approvisionnement, Stockage, Logistique des RLD

  • Livraison mondiale - Chaîne du froid/température

  • Enregistreurs USB contrôlés - porte à porte, CIF, Ex-works

  • Approvisionnement sécurisé et confidentiel

  • Documentation produit Certificats d'origine (COO) de la Chambre de commerce de Victoria. 

  • Approvisionnement mondial en produits biologiques

  • Produits hospitaliers complexes difficiles à trouver

  • Certification des comparateurs par notre Qualified Responsible Person (QRP) - Pharmacien.  

  • Fiable, audité avec SOP's 

  • Taux de réponse rapide avec les fuseaux horaires australiens et  européens couverts dans les deux régions (Melbourne Australie et Varsovie Pologne) 

  • RLD humain et IMP 

  • Sites de stockage sous licence à Melbourne et en Pologne 

  • Leki porównawcze do badań klinicznych z przedstawicielem w Polsce

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