Newsletter | August 2, 2019

08.02.19 -- Five Factors To Consider When Managing Clinical Supplies For Asia-Pacific Studies

Five Factors To Consider When Managing Clinical Supplies For Asia-Pacific Studies

In addition to careful adherence with all applicable regulatory and customs requirements, sponsors should understand and be sensitive to the cultural and business norms of each country included in their study. By being patient and listening to the local needs, clinical trials can run smoothly across the Asia-Pacific region.

An Innovative Solution To Flexibly Meet Unique Primary Packaging Requirements

Child-resistant blister packaging requirements were necessary for a global Phase III study. A flexible design was created with an integrated blister card that could also support larger study requirements of 1.9 million monthly dosing cards. Through customized commercial blistering equipment, a solution was developed that would accommodate the customer’s growing demands for clinical supplies.

Key Considerations When Sourcing Reference Products For Biosimilar Studies

In order to ensure a smooth development and clinical process, companies must carefully plan their activities with regard to the innovator biopharmaceutical. If research, development, and clinical strategies are planned under the assumption that the innovator drug will function like a commodity, the final product may not be executable.

Demand-Led Services And Clinical Supply Efficiency

Demand-led supply is designed to meet the needs of patients, clinical sites, clinical teams, and sponsors. See how this service can benefit you with shorter lead time, less waste, less stock out risk, and no booklet labels.