Comparator / RLDs and Clinical Trial Ancillaries
At Pro Pharmaceuticals Group, we are experts in sourcing high-quality comparator and reference-listed drugs (RLDs) for clinical trials worldwide. Since 2015, we have been a trusted partner, ensuring research organizations have reliable access to the pharmaceuticals they need. With a focus on precision, compliance, and reliability, we provide tailored solutions and exceptional service to advance clinical research globally.
Why Choose Pro Pharmaceuticals Group?
Since 2015, Pro Pharmaceuticals Group has been a trusted partner in delivering superior pharmaceutical solutions. We provide seamless procurement and distribution across over 30 countries, ensuring compliance with Australian GDP and ISO 9001 standards, as well as European GDP and GMP certifications. Our advanced cold chain systems ensure product safety and reliability, while our extensive experience in navigating complex regulatory requirements allows us to deliver tailored solutions with responsive service across multiple time zones. We are committed to offering competitive pricing without compromising quality, making us the ideal partner for your clinical research needs.
With a secure supply chain that includes comprehensive product documentation and rigorous quality checks at every stage, Pro Pharmaceuticals Group provides peace of mind to clients, simplifying the complexities of clinical trial sourcing.
Delivering Quality and Reliability in Clinical Pharmaceuticals
Leadership
Global Expertise
Pro Pharmaceuticals Group's leadership in pharmaceutical solutions, backed by our established global partnerships and industry insights, positions us as a trusted partner in comparator sourcing.
We offer a solution. With licensed facilities in Melbourne, Hamburg, and Warsaw, and over a decade of experience, we provide global comparator sourcing that ensures secure, efficient, and reliable access to the products you need.
Leveraging a vast supplier network spanning over 30 countries and utilizing multiple depots and warehouses worldwide, we streamline the process from manufacturer to destination. Our expertise and dedicated support help you navigate the intricacies of international regulations and logistics, reducing the time and cost associated with drug development. From sourcing to delivery, we manage the entire process, maintaining integrity and compliance at every step.
Tailored Clinical Trial Solutions
Trust & Quality
Clinical trials demand precision and reliability, particularly in sourcing comparator drugs. Navigating regulatory requirements, ensuring supply chain integrity, and maintaining reliable access to high-quality products are significant challenges that can delay drug development and create logistical and regulatory hurdles.
Quality is at the heart of Pro Pharmaceuticals Group. Our unwavering dedication to compliance ensures all products meet rigorous standards, including Australian certifications such as GDP and ISO 9001, as well as European certifications including EU GDP and EU GMP for secondary labeling and QP release. Our advanced cold chain systems safeguard product integrity throughout the entire process, from procurement to delivery. These robust practices guarantee your clinical trial supplies meet the highest industry benchmarks, ensuring the integrity and security of every product.
"The quality control measures and timely delivery from Pro Pharmaceuticals Group were impressive. Their commitment to compliance and reliability makes them our go-to supplier for comparator drugs."
R&D Lead at Netherlands based Pharmaceutical Company.
"Pro Pharmaceuticals Group provided us with the hard-to-find comparators we needed quickly and efficiently. Their service was exceptional, ensuring our clinical trial stayed on schedule."
Head of Clinical Trials Services German CDMO
"Working with Pro Pharmaceuticals Group has been a game-changer for our clinical trials. Their extensive network and expertise in sourcing rare comparator drugs have significantly streamlined our process."
Manager - Strategic Sourcing Leading Generic Manufacturer in India.
Simplify Clinical Trial Sourcing Today
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
