Meet Our Regulatory Affairs Team

As Head of Regulatory Affairs, I bring over 20 years of experience in regulatory affairs for human medicinal products. Throughout my career, I have developed extensive expertise in regulatory lifecycle management, including dossier preparation and maintenance, variations, national procedures, MRPs and DCPs, as well as strategic regulatory planning and compliance oversight. I also have experience with CE technical documentation for medical devices.

Known for my calm, collaborative and pragmatic approach, I build strong relationships with clients, health authorities and internal stakeholders to deliver effective regulatory solutions. Passionate about regulatory excellence, I enjoy guiding teams, driving continuous improvement and helping our organisation successfully navigate an evolving regulatory environment.

I am a Regulatory Affairs Manager, Pharmacist, with over 19 years of experience in Regulatory Affairs, Pharmaceutical Development and Quality Assurance. After graduation in Pharmaceutical Sciences at Utrecht University, I started my career at Dechra Veterinary Products (2007 – 2015). As a project leader, I managed to develop many veterinary medicinal products and registered them throughout the world in a GMP environment. Furthermore, as a Qualified Person I was responsible for batch release. In the meanwhile, I gained my PhD in Pharmaceutical Sciences (2009 – 2014), where I evaluated the risk of fractures in patients with neurological disorders. I continued my career at Ducares (a TNO initiative) (2015 – 2017), where I co-developed complex analytical methods and cooperated in several projects to enhance human and animal safety. I returned to regulatory affairs at Interchemie werken “De Adelaar” BV (2017 – 2019), being responsible for obtaining and maintaining veterinary registrations worldwide. Since June 2019, I work at Interdos, where I co-developed and registered several human medicinal products for different customers.  I would like to describe myself as someone with a strong perseverance, structured, independent, precise and as a strong team player who maintains overview in complex situations. I am looking forward to cooperate with you.

Not long after completing my studies in biotechnology with a master in medical/molecular biotechnology at Wageningen University I started working as an regulatory affairs officer at Interdos. After 9.5 years of working as an RA officer and RA manager, learning and getting experience in the different aspects of regulatory affairs I transferred to my current function of Regulatory Affairs Specialist.

I am an Organic Chemist (BSc) with over 25 years of experience in the human pharmaceutical industry. I started my career as an R&D Project Assistant at MSD (formerly Organon) before transitioning to Regulatory Affairs, where I coordinated and supported regulatory submission procedures across Europe. Since May 2015, I have been working at Interdos Pharma, providing regulatory services to a wide range of clients. My experience varies from maintaining, updating, and reviewing eCTD dossiers to coordinating variations, national procedures, MRPs and DCPs. I am a cooperative, enthusiastic, and results-oriented professional who enjoys supporting others and contributing to successful team outcomes.

With a background in cardiovascular and oncology research, I transitioned to the pharmaceutical industry in 2014. Since then, I have built extensive experience in GMP and quality assurance, developing a strong understanding of pharmaceutical compliance and quality systems.

Since joining Interdos in 2021 as a Regulatory Affairs Officer, I have been responsible for ensuring that medicinal products comply with national and international regulatory requirements. I stay up to date with evolving legislation, guidelines, and industry practices to support successful product maintenance and lifecycle management.

 I am an accurate, well-organized professional who values collaboration and strong relationships with colleagues, customers, and regulatory authorities.

I chose to study Pharmacy by literally pulling the profession from a hat but after completing my Bachelor of Pharmacy at Rhodes University in South Africa and discovering the magic in the science of medicine, I have never looked back.

As an Organic Chemist (BSc), I have always been passionate about the pharmaceutical industry and improving patients’ health. With over 10 years of experience in quality-related roles within GMP and non-GMP environments, I joined Interdos as a Regulatory Affairs Officer. I have experience with regulatory submissions and lifecycle management, dossier maintenance, EMA, ICH and GMP compliance, plus labeling and artwork review. I am a pragmatic, reliable and analytical professional who enjoys helping clients find practical solutions to regulatory challenges.

Upon completing her degree in Biochemistry at University of Cape Town, Gloria realized that a laboratory career was not her path. Shortly after graduation, she seized an opportunity to join a graduate program in Regulatory Affairs in Cape Town, South Africa. This marked the beginning of Gloria’s journey in the pharmaceutical field, a domain where she can pursue her passion for healthcare.

I completed degrees in microbiology and virology in South Africa and worked as a laboratory analyst in the United Kingdom before I embarked on my pharmaceutical journey. After completing my pharmacy degree I worked as a retail and hospital pharmacist. I then discovered the exciting and challenging world of regulatory affairs. I have over ten years of experience within the dynamic and ever evolving pharmaceutical regulatory field. I have knowledge of a broad product base, ranging from oral dosage forms to sterile injectables, of which many are globally marketed. As a result, I have a unique knowledge and experience in managing the complexities of various regulatory authorities simultaneously, ensuring that multiple regulatory compliance requirements are met. I am involved in collaborating with cross-functional teams to implement regulatory and compliance strategies and execute development projects, ensuring that manufacturing sites are ready and compliant prior to regulatory approval and implementation. I stay informed of regulatory changes and updates in order to advise and prepare clients proactively of any regulatory risks. I also contribute to resolving regulatory queries, managing variation strategies and general product lifecycle management. Joining Interdos in 2024, I am looking forward to apply my skills and knowledge within this exciting new environment. I am eager to engage with clients and customers and to assist with their regulatory needs and requirements.

Experienced Registration Manager with a strong focus on regulatory affairs in the pharmaceutical industry. Specializes in regulatory submissions, ensuring compliance with FDA, EU/EEA regulations, and ICH guidelines while managing the entire product registration process across various markets. Proven track record in lifecycle management, overseeing pharmaceutical products from development to market entry. Proficient in GMP/GDP and risk assessment, with skills in regulatory strategy development and cross functional team management, complemented by strong analytical skills and attention to detail. Possesses expertise in data management and project coordination, with experience across diverse markets, including EU, ASEAN, LATAM, MENA, APAC. Passionate about improving regulatory practices and seeking opportunities to make a significant impact in the pharmaceutical sector.