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All drugs and medical devices must be accompanied by extensive and complex product information. This is highly regulated because any mistake or error could threaten patient safety and outcomes.
17-19 May 2022
The challenges confronting the clinical trial supply chain in light of the COVID-19 pandemic are without precedent. With delays and disruption continuing to affect trials around the world, and regulatory changes impacting operations, the resourcefuln
Event Ended
Belgium
Paid
Brussels