Clinical Trials

GMP compliant Services for Pharmaceutical Trials

Activoris received the manufacturing and import license for secondary packaging of clinical samples. The authorization includes non-sterile drugs, biologicals, human or animal extracted products, hormones, prostaglandins, cytokines as well as immune-suppressives for phase I, II, and III clinical trials. Your trial is a challenging project, rely on our expertise to establish the right strategy regarding to purchasing, kit configuration and supply to your study centers.

  • Flexible Project Support, Partner-Network for primary packaging
  • Kit Configurations, Booklets, Package Inserts
  • Cooling Capacities 2 – 8 °C, Hazardous Substances
  • Packaging and Labeling, Kit Assembly
  • QP Release, GMP compliant Conduct and Documentation
  • Storage and Distribution

Medtech Studies

Today, the requirements for clinical trials gain more importance in view of the approval of innovative devices. However, a CE-marking or a 510(k) clearance is not enough to achieve sales. The increasing price pressure calls for a superior differentiation. Meaning, obtaining re-imbursement requires to effectively demonstrate superior performance of your device. Our medtech and pharma experience of multiple clinical developments and a specialized provider network navigate you through this important development step.

  • Clinical Strategy and overall Coordination
  • Tenders, CRO-Selection
  • Manuals, Device Trainings
  • Device Assembly
  • Clinical Trial Logistics