OUR SERVICES

For the first time, clinical supply management is being offered in the spoken language, suited to the local culture and in close proximity to the manufacturing site.

From receipt of raw materials through distribution to study depots, inPACK manages and oversees the entire process of the study kit production. We maintain, with utter transparency, the highest standards of quality.

Proper handling of your investigational medicinal product is a key factor in the clinical trials success

Coordinating all activities related to clinical supplies management set up and maintenance:

• Writing the clinical supplies chapter in the study protocol
• Statistical services and creating Randomization lists
• Designing the study kit according to study protocol
• Inventory planning; Ongoing reporting of inventory levels and alert the need for repeat packages
• Writing, editing, designing and translating labels and accompanying documents
• Design and manufacture of printed packaging materials (such as labels and multi - lingual booklets)
• Importing of investigational medicinal and Comparators
• Testing of Printed packaging Materials
• Secondary packaging
• Clinical batches release by an authorized Qualified Person (QP) by the Israeli Ministry of Health.
• Storage under controlled conditions (-15°c to -25°c, 2°c to 8°c and at room temperature 15°c to 25°c)
• Controlled delivery of study kits
• European QP services
• Locating and linking global dispensary according to the study sites
• Provider selecting for IVRS/IWRS, system characterization and project management

Our Advantages:

• High and uncompromising quality standards, while providing customized solutions for clinical trials Sponsor’s needs
• Knowledge and professional experience in managing clinical trials supplies, at all stages of the experiment, from first phase trials to complex ones, global, double-blind, etc.
• Easy accessibility
• Attractive costs