RQM+ is a global MedTech service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market.

Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our: 
• Regulatory and Quality Consulting
• Lab Services (Jordi Labs)
• Clinical Trials
• Reimbursement
• Technology Solutions


RQM+

Women’s health is finally getting the attention it deserves, yet progress is still slowed by gaps in clinical trial diversity, complex regulatory pathways, and funding challenges.

In this RQM+ Live! panel discussion, industry leaders and regulatory experts will share real-world strategies MedTech companies can use to navigate these barriers and bring life-changing innovations to market.

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### **Why Attend?**

*   **Unlock Market Opportunities** – Women’s health is one of the fastest-growing MedTech sectors, with rising investor interest and funding.
*   **Gain Regulatory Insights** – Understand how evolving regulations impact clinical trials, approvals, and commercialization.
*   **Learn from Real-World Success** – Hear how industry leaders are overcoming challenges and making an impact.
*   **Ask Your Toughest Questions** – Engage directly with panelists during the live Q\&A.
*   **Bring Innovations to Market** – Get expert insights on bridging clinical research, regulatory approval, and commercialization.

### **Discussion Topics**

*   **The Business Case for Women’s Health Innovation** – Why investors, manufacturers, and regulators are prioritizing this space and what it means for MedTech companies.
*   **Clinical Trials and Data Gaps** – The urgent need for inclusive research, historical data biases, and evolving regulatory expectations.
*   **Regulatory and Market Access Hurdles** – Key challenges in securing approval and reimbursement—and how to overcome them.
*   **Scaling Women’s Health Solutions** – Lessons from industry leaders on funding, partnerships, and commercialization strategies.

### **Who Should Attend?**

*   MedTech professionals driving innovation in women’s health
*   Regulatory and quality leaders navigating complex approval pathways
*   Clinical trial specialists improving diversity and data accuracy
*   Investors and strategists seeking insights into funding and market growth
*   R\&D and product development teams designing women’s health solutions
*   Healthcare policymakers and advocates shaping the future of women’s health innovation

**Panelists and moderator:**

*   Marissa Fayer – CEO, Her Health Equity & DeepLook Medical
*   Megan Callanan – US & Global Regulatory Lead, Natural Cycles
*   Stephanie Kladakis – Executive Vice President, Chief Technology and Regulatory Officer, AgNovos Bioscience
*   Alexia Haralambous – Senior Principal, RQM+
*   Jaishankar (Jai) Kutty, Ph.D. – Vice President, Global Regulatory Affairs, RQM+ (moderator)

*Certificate of Participation available upon request for live attendees.*
