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"After leading major operational workstreams within a $10M+ pharma account at Freeman and building operational success across roles at Roche, I founded
The Attic Muse to help companies access Fortune 500-caliber strategy
and execution." - Helen
Helen drives overall strategy and growth for our clients. Her decades worth of experience has been in Fortune 500 companies, other industry leaders, and startups all within the Diagnostics, Pharmaceutical, Manufacturing, Baking, Construction, Restaurant, and Experiential Marketing,
Events, and Exposition industries.
She provides tailored solutions that give results, enhance efficiency, and improve overall performance. She drives organizations to optimize their operations, increase revenue, and achieve their strategic objectives.
With a proven track record of success, she brings a unique blend of analytical expertise, creative problem-solving skills, and humor to every project.
Helen understands the importance of staying ahead of the curve and adapting to rapidly changing market dynamics. Whether it's developing a comprehensive plan, improving business operations, or executing a successful event, she works closely with her clients to understand their unique needs and goals and then crafts customized solutions that exceed expectations. She prides herself on being honest, results-oriented, and dedicated to delivering tangible outcomes that make a real difference.
Helen has served on multiple industry and non-profit association boards, is an industry expert and public speaker, and is proud of the work she has done to raise millions for various non-profit organizations.
Helen holds a BA in Corporate Communication with a Minor in French from Walsh University, and a MSc in Business & Management from Aston University UK. She maintains a Healthcare Compliance Certificate from St. Louis University, and was one of the first in the industry to recieve this designation. She is further pending award of CTSM and aPHR Certifications. Helen is fluent in English & Greek and intermediate in French.
In her free time she enjoys taking cruise vacations, volunteering, taking bike rides with her family, attending comedy shows, and laying in a hammock listening to music while reading a good book.
You can email her directly below and connect with her on LinkedIn - https://www.linkedin.com/in/kalorides

"After 15+ years leading global regulatory affairs at Sekisui, Abbott, BD, and other companies, I saw an opportunity to bring that strategic expertise directly to companies navigating FDA pathways without the overhead of full-time executive hires." - Dimitris
Dimitris drives regulatory strategy and quality excellence for our clients. With over 15 years of leadership experience, he has lead teams in industry-leading organizations including Abbott, Roche Diagnostics, Sekisui Diagnostics, Becton Dickinson (BD), and others, as well as supporting innovative startups in the Medical Device, Diagnostics, and Medical Software sectors.
He specializes in developing and executing regulatory pathways that secure FDA and global approvals efficiently, designing robust Quality Management Systems, and ensuring products meet the highest standards of safety and compliance. Dimitris combines deep technical expertise with strategic insight to help companies bring their products to market faster while maintaining full compliance and operational integrity.
Throughout his career, he has led complex submissions for Class I - III devices, built and transformed quality systems to meet ISO 13485 and 9001 standards, and driven digital transformation initiatives that streamline regulatory operations and enhance data accessibility.
Known for his proactive approach and collaborative leadership style, Dimitris works closely with clients to navigate regulatory challenges with confidence. He is passionate about creating practical solutions that align with business objectives and regulatory requirements, ensuring organizations remain agile, compliant, and positioned for growth.
Dimitris holds a BA in Molecular Biology & BioChemistry with a Minor in Economics from Rutgers University, an MBA from IUPUI, and a Clinical Research Certificate from IUPUI, along with countless hours of continued professional development. He is a member of RAPS, a published researcher, and holds technical proficiencies in FDA, ISO 13485/9001/27001, EU Guidelines & Regulations. Dimitris is also fluent in English & Greek.
In his free time, Dimitris enjoys exploring new technologies, reading, mentoring emerging regulatory professionals, cooking Mediterranean dishes, and spending time with his family and pets.
You can email him directly below and connect with him on LinkedIn – https://www.linkedin.com/in/dimitrisdemirtzoglou
We are intentionally structured to endure beyond any single engagement.
Our advisory work is delivered through documented frameworks, standardized decision models, and disciplined operating processes that preserve quality as the firm grows.
Senior specialists are engaged through a vetted network if required for specific tasks, ensuring continuity without diluting leadership oversight.
This structure allows us to scale selectively while maintaining the principal-led quality our clients expect.
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