Dane Popovski
Senior Director Regulatory Affairs at BD | Chicago, Illinois, United States
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Dane Popovski serves as Principal at Abiolex, where he plays a pivotal role in advancing the scientific and commercial objectives of medical technology companies on a global scale. With a robust background in biomedical engineering, Dane leverages his expertise in regulatory guidelines and quality systems to navigate the complex landscape of Class III medical devices and combination products. His deep understanding of the intricacies involved in medical device development allows him to provide invaluable insights to clients, ensuring compliance with stringent regulatory standards while fostering innovation.
At Abiolex, Dane is currently spearheading several key projects aimed at enhancing stakeholder engagement and optimizing auditing processes for emerging medical technologies. His ability to communicate effectively with diverse stakeholders—ranging from engineers to regulatory agencies—ensures that all parties are aligned and informed throughout the product lifecycle. This interpersonal skill set not only facilitates smoother project execution but also cultivates long-lasting relationships that are essential for success in the lifesciences sector.
Dane's commitment to advancing medical technology is evident in his proactive approach to problem-solving and his dedication to continuous improvement. By integrating cutting-edge biomedical engineering principles with strategic regulatory insights, he empowers companies to bring innovative solutions to market efficiently and effectively. As the medical technology landscape continues to evolve, Dane Popovski remains at the forefront, driving progress and shaping the future of healthcare innovation through his work at Abiolex.
Senior Director Regulatory Affairs at BD in December 2024 to Present
Principal at Abiolex in January 2022 to December 2024
Chief Operating Officer at Dilon Technologies Inc in July 2017 to October 2021
President - Management Consulting at illumireg inc. in January 2013 to December 2017
Principal Consultant at Fresenius in March 2013 to November 2015
Medical Devices & Combination Products at Baxter Healthcare in June 2012 to March 2013
Medical Devices at Cardiac Science Corporation - Criticare Systems Inc. in March 2011 to June 2012
Medical Devices / In Vitro Diagnostics at Thermo Fisher Scientific in June 2010 to March 2011
Startup - Molecular Biology / Genetic Engineering / Precision Medicine at MCW Biotechnology and Bioengineering Center in June 2009 to June 2010
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Regulatory Guidelines
Recalls
Organization Skills
Strategy
Global Regulatory Compliance
Communication
Product Quality
Negotiation
Presentation Skills
Regulatory Compliance
Stakeholder Engagement
Quality Management
Auditing
Combination Products
Class III Medical Devices
Project Management
Quality Assurance
Quality Control
Class II
Regulatory Strategy
Technical Documentation
Relationship Building
Interpersonal Skills
Strategic Thinking
Regulatory Requirements
Regulatory Filings
Regulatory Approvals
Risk Management
Regulatory Affairs
ISO 13485
ISO 14971
IEC 60601
IEC 62304
Quality System
FDA
Medical Devices
Regulatory Submissions
CAPA
Design Control
Lifesciences
V&V
Quality Auditing
Product Development
Cross-functional Team Leadership
Change Control
Biomedical Engineering
Validation
Leadership
ISO
CE marking
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Discover more about BDWhat is Dane Popovski email address?
Email Dane Popovski at [email protected]. This email is the most updated Dane Popovski email found in 2026.
How to contact Dane Popovski?
To contact Dane Popovski send an email to [email protected].
What company does Dane Popovski work for?
Dane Popovski works for BD
What is Dane Popovski's role at BD?
Dane Popovski is Senior Director Regulatory Affairs
What is Dane Popovski's Phone Number?
Dane Popovski's phone (217) ***-*166
What industry does Dane Popovski work in?
Dane Popovski works in the Government Relations Services industry.
Dane Popovski Email Addresses
Dane Popovski Phone Numbers
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