Gustavo Marco

Director, Global Regulatory CMC at GSK

He received a Pharmacy Degree (PharmD equiv.) from Valencia University (Spain) and a Masters Degree in Industrial Pharmacy from CESIF in Barcelona (Spain).
Gustavo started his career working for almost 6 years in product development and quality assurance positions across a wide range of products in both Spain and the UK.
In 2006, Gustavo joined the MHRA where he worked for over 7 years. First as Senior Assessor and then as a Team Manager in the Respiratory, Dermatology and Ophthalmology department.
During his time at the MHRA, Gustavo was responsible for the assessment of a number of QbD applications. He was also responsible for the Scientific Advice delivery of the department.
Gustavo is currently a Director of Global CMC Regulatory Affairs at GSK and the regulatory subject matter expert on QbD.

Membership, structure, strategic priorities, overview of workstreams, accomplishments and impact