Our Mission
Streamlining your clinical trial submissions, managing lifecycle changes, and ensuring global compliance with tailored CMC solutions.
Founder
Aosaf is a seasoned Regulatory Affairs CMC expert with extensive experience across small molecules, biologics, vaccines, and radiopharmaceuticals. He specialises in developing regulatory strategies, preparing high-quality submissions, and managing lifecycle activities to ensure compliance with global regulatory standards.
Known for his collaborative approach and deep technical knowledge, Aosaf helps clinical-stage pharmaceutical companies navigate regulatory complexities efficiently. He is passionate about bringing high-quality treatments to market. Reach out to learn how his expertise can support your regulatory success.