Understanding the regulatory landscape and building robust clinical evidence for nutraceutical product claims across EU and MENA markets.
Key success factors and strategic considerations for launching pharmaceutical products in today's evolving regulatory and market landscape.
Key changes, timelines, and actionable steps for ensuring full compliance with the European Medical Device Regulation.
Market analysis, regulatory environment, and strategic considerations for pharmaceutical companies entering Middle East and North Africa.
Real-world case study examining challenges, solutions, and best practices in transferring biologics manufacturing technology.
Strategic framework for balancing scientific innovation with operational execution to maximize product development success.