EVENT INTELLIGENCE PLATFORM

Medical Device Regulatory and Quality Summit 2025 Attendee List

Tap into the sample of the enriched attendee list for Medical Device Regulatory and Quality Summit 2025 to connect with strategic voices, uncover sponsor details, and explore verified emails across top-tier companies. This data is sourced via Vendelux, combining organizer inputs and predictive modeling to support smarter event outreach.

Maximize Your Impact At Medical Device Regulatory and Quality Summit 2025

Medical Device Regulatory and Quality Summit 2025, scheduled for August 21 in New Delhi, offers a high-value platform for senior executives operating in the medical device sector, particularly those focused on compliance, clinical evaluation, safety, and quality systems. Attendees will include regulatory affairs leaders, quality management professionals, compliance officers, and governmental policy influencers shaping the future of medical device oversight in India and across Asia.

Many on-site conversations at this summit drive decisions around supplier selection, operational benchmarks, and market expansion strategies. Buyers and leaders attending this event actively evaluate technologies, services, and consulting partnerships to meet MDR, ISO, and CDSCO requirements, presenting opportunities for organizations looking to align their solutions to regulatory priorities. With access to the enriched attendee list from Vendelux, sales and go-to-market teams can engage early with industry compliance leads and product safety heads, often holding direct or influential budget ownership. Early connections matter, especially when regulations shift rapidly, and trust with domain experts drives long-term adoption.

How Sales, Marketing And Revops Teams Can Use This Attendee List

This event brings together well-informed, regulation-focused buyers with a strong interest in operational reliability and long-term compliance. Using Vendelux’s enriched conference attendee list helps your team move from generic outreach to data-supported relationship building.

Segment contacts by company type—manufacturers, distributors, testing labs, and regulators—and align messaging to their compliance roles, whether tasked with audits, submissions, or product certifications. Target quality heads who lead evaluation of regulatory platforms or external GMP consultants who influence purchasing decisions. Connect with regulatory affairs executives before the summit to introduce your value in helping them meet evolving safety requirements or reduce product-to-market delays.

The enriched data can help schedule meetings in advance with policy influencers and mid-size device firms before their annual budget cycles close. Use detailed attendee data—roles, company sites, and verified contact methods—to send timely offers and follow up post-summit with insight-driven campaigns connected to shared onsite discussions. Knowing how to get more meetings and using the attendee data meaningfully increases the chances of turning initial contact into strategic opportunities.

Timing Is Everything

Medical Device Regulatory and Quality Summit 2025 will take place on August 21, 2025. With just a few months remaining before the event, it’s the right time to use the Vendelux platform to identify potential decision-makers and initiate pre-event outreach.

Early connection is key when targeting compliance professionals, as Q3 evaluators often lock in procurement partners and finalize solution assessments by late summer. Use the enriched attendee list to prioritize accounts, customize messaging for regulatory leads, and propose mid-year strategy meetings tied to their program timelines. Reaching out now positions your offering in front of decision-makers who shape how their organizations interpret and act on new compliance obligations.

What’s Included In The Medical Device Regulatory And Quality Summit 2025 Attendee List?

Vendelux provides visibility into executives expected to attend Medical Device Regulatory and Quality Summit 2025 through a blend of organizer-supplied data and predictive tools. Clients can upload a list of key accounts to find overlapping attendees and plan strategic outreach accordingly.

The enriched list includes first and last names, job titles, company names, company websites, city, state, country, LinkedIn profiles, verified email addresses, and phone numbers when available.

Where Is Medical Device Regulatory And Quality Summit 2025?

Hotel Pride Plaza | New Delhi, Delhi, India.

When Is Medical Device Regulatory And Quality Summit 2025?

August 21, 2025.

What Type Of Event Is Medical Device Regulatory And Quality Summit 2025?

Medical Device Regulatory and Quality Summit 2025 is a specialized industry event tailored to professionals responsible for product compliance, clinical safety, regulatory systems, and quality assurance in the medical device sector. The event features keynote sessions from regulatory authorities, expert-led panels, and interactive networking discussions for industry peers and government regulators.

How Many People Attend Medical Device Regulatory And Quality Summit 2025?

The summit is expected to host around 150 to 200 attendees, primarily from across India and select regions in Southeast Asia. The audience is composed of senior-level professionals from medical device manufacturers, global regulatory consultants, and leaders from standards organizations and health authorities.

Unless expressly stated, Vendelux is not endorsed by, affiliated with, authorized by, or in any way officially connected to any event organizer or any of its subsidiaries or affiliates. All product and company names are the registered trademarks of their original owners. The use of any trade name or trademark not owned by Vendelux is for identification and reference purposes only and does not imply any association with such trademark holder.
 
If you are the organizer of this event and wish to provide the complete attendee list for this event to help ensure the accuracy of our data, please contact our Organizer Partnerships team. Submission of attendee information is voluntary and subject to verification. By providing this data, you represent that you have the legal right to share such information and that doing so does not violate any applicable laws, privacy policies, or contractual obligations.
 

Vendelux effortlessly booked over 20 meetings with our core ICP stakeholders across two events - more than triple what we were able to do on our own.

Aaron Bollinger

Chief Revenue Officer (CRO), Voltage

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