David McDonough is a transformative executive leader in the medical device and healthcare technology industries, recognized for his ability to drive business growth, operational efficiency, and product innovation. As president of Northgate Technologies, Inc., he spearheaded a remarkable turnaround, increasing revenue from $7 million to $21 million and improving EBITDA from a $500,000 deficit to $5 million within five years—achieved without additional capital investment. With over 33 years of experience, McDonough has successfully led market expansions, secured multimillion-dollar contracts, and brought award-winning medical technologies to market. His expertise spans strategic planning, sales and marketing, product development, and stakeholder engagement, making him a sought-after leader in the industry. A dynamic communicator and thought leader, he has shared his insights at international conferences such as MedTech World in Malta and Houston. Now seeking board roles, McDonough is eager to leverage his vast experience to help organizations scale, optimize operations, and achieve industry leadership.

As a physician-scientist and biotech executive, I have dedicated my career to bridging the gap between groundbreaking medical research and commercial success. From securing multimillion-dollar funding to leading strategic M&A deals, my passion lies in driving healthcare innovation that delivers real-world impact. Here is my biography.

Excited to share my professional biography, highlighting my journey in the medical device industry, my expertise in quality systems and regulatory compliance, and my passion for driving innovation in healthcare technology. With over a decade of experience, I continue to focus on advancing medical devices through strategic quality initiatives and global regulatory alignment.

With over 35 years of experience in the healthcare industry, I’ve dedicated my career to building high-performing teams, driving commercialization strategies, and fostering strong company cultures. As a board member, advisor, and executive leader, I thrive on delivering breakthrough growth and creating lasting impact. If you’re looking for strategic leadership in medical devices, pharmaceuticals, or life sciences, I’d love to connect. Here is my biography.

I’m excited to share my executive biography, highlighting my experience in R&D, regulatory strategy, and product innovation within the medical device industry. As I transition into board and advisory roles, I look forward to leveraging my expertise to help med-tech companies scale, innovate, and navigate regulatory landscapes.

Frank Pokrop is an accomplished leader in regulatory affairs and quality assurance, bringing over 15 years of expertise across medical devices, software/SaMD, capital equipment, and injectable drugs. Certified in multiple disciplines, including RAC, CQE, CQA, CSQE, and CPGP, he has successfully navigated complex global regulatory landscapes, overseeing product approvals and quality management systems for leading organizations such as Abbott, BD, CareFusion, and QuidelOrtho. Renowned for his strategic mindset and collaborative approach, Frank has led global compliance programs across 48 sites, driven cost reductions exceeding $3 million annually, and served as a trusted regulatory liaison for corporate boards and international agencies. A results-oriented executive with a passion for developing teams and achieving excellence, Frank is now seeking a senior position in regulatory affairs or quality assurance to further his impactful career.

Excited to share my professional journey in NGS cancer diagnostics, biotech, and healthcare innovation! With over 20 years of experience spanning product management, AI-driven automation, clinical trials, and regulatory compliance, I have led multi-billion-dollar product launches and driven transformative advancements in precision medicine and oncology. My expertise in agile methodologies, strategic planning, and cross-functional leadership has enabled me to bridge science and business for impactful solutions. Here is my biography.

Eric Grott is a dynamic executive with over 25 years of experience driving financial excellence, operational efficiency, and strategic growth across startups, manufacturing, distribution, and medical device industries. Known for his ability to deliver transformative results, Eric has led multimillion-dollar initiatives, streamlined operations, and embedded data-driven decision-making practices to create scalable success. Currently serving as CFO/COO of Power/mation, Eric has been instrumental in aligning organizational strategies, achieving record growth, and enhancing profitability, all while maintaining a hands-on, collaborative leadership style. His commitment to innovation and value creation makes him a sought-after leader in the business landscape.

Jon J. Ahola is a seasoned executive with nearly three decades of experience driving innovation and operational excellence in the medical technology industry. Currently serving as Vice President of Global Research and Development for Stryker's Trauma & Extremities Division, Jon has led the development and successful launch of over 40 groundbreaking medical products, ranging from implants to digital software applications. His leadership was pivotal in the integration of Wright Medical, Stryker's largest acquisition to date, and his influence extends globally through roles that have spanned Europe, Asia, and North America. Guided by a commitment to integrity, teamwork, and his mission to "make humanity better," Jon combines technical expertise with visionary leadership to transform healthcare and improve lives worldwide.

Tina Liedtky is a seasoned executive with over 20 years of experience driving innovation and growth in the healthcare, medical devices, and diagnostics industries. Renowned for her expertise in commercialization strategies, operational excellence, and global market leadership, Tina has held pivotal roles shaping organizations that serve over 60 countries. A passionate advocate for improving patient outcomes, she combines strategic vision with hands-on leadership to help companies achieve new levels of success. Tina is also an accomplished speaker, regularly sharing her insights on diagnostics innovation and women’s leadership at major industry conferences. Guided by her mission to make an impact on patients' lives, Tina is dedicated to advancing healthcare solutions that help people live longer and healthier lives.

I’m excited to share my professional journey and insights as a Sales & Marketing Leader with over 40 years of experience driving revenue growth, transforming strategies, and building top-performing teams. My passion lies in empowering organizations to achieve lasting success through innovation, strategic planning, and leadership development. Here is my biography.

Michael Ekstut is a seasoned business leader with over 30 years of experience in the life sciences industry, specializing in drug discovery, development, and regulatory strategy. He has held senior leadership roles at industry-leading companies, including Certara, where he guided the company’s commercial and product strategy in the regulatory and access sector. Michael is known for his strategic vision and ability to drive innovation, optimizing clinical development programs and supporting biopharma companies in navigating complex regulatory landscapes. His deep expertise in business consulting, technology, and operational management has enabled him to successfully advise executives and investors across pharmaceuticals, biotechnology, and medical devices. Currently serving as a Senior Advisor at InSilicoTrials, Michael continues to leverage his vast experience to help organizations maximize the impact of their clinical development programs and investments.

Darren LaCour Jr. is a seasoned expert in biomedical product development, with a distinguished career focused on ensuring regulatory compliance and patient safety. His extensive knowledge in clinical trial design, execution, and oversight has been pivotal in bringing innovative medical devices to market. As a strategic leader, Darren has successfully navigated the complex processes required for U.S. regulatory approval, while also dedicating himself to educating future leaders in the field. His commitment to excellence and mentorship has made him a respected figure in both industry and academia.

I am excited to share my professional journey, reflecting over 27 years of experience in the pharmaceutical and biotech sectors. From co-founding Vidara Therapeutics to leading commercialization efforts at Horizon and AVM Biotechnology, my passion for innovation and growth has been at the core of my work. Here is my biography.

Tom Fourt is an accomplished marketing executive with over 20 years of experience in marketing strategy, product innovation, market research, lifecycle management, and digital...

I'm excited to share my journey in the life sciences sector! With over 39 years of experience leading risk management strategies for FDA-regulated companies, I’ve had the opportunity to help businesses navigate complex risks and regulatory challenges across industries like medical devices, biotech, pharmaceuticals, and clinical trials. At Hylant, I lead a team dedicated to building tailored risk management frameworks that allow our clients to focus on innovation while we manage the evolving market complexities. Integrity, perseverance, and paying it forward are values that have guided me throughout my career, and I’m passionate about supporting businesses as they grow and succeed in a distracted world. Let’s connect and explore how we can collaborate to protect and grow your business!