International Conference on Medical Devices, Innovation & Regulation .

International Conference on Medical Devices, Innovation& Regulation

Date:17th & 18th June 2026 | Time: 8.00 am – 12:00 pm (IST) | Location: Online

Sample Abstract

Phone: 8977760443 Email: support@onegrasp.com

Dr. Santosh Kumar Mishra

Role: Independent Researcher (Scholar)
Department: Population Education Resource Centre, Department of Lifelong Learning & Extension
University: S.N.D.T. Women’s University
Country: India

Dr. David Wortley

Role: Non-Executive Director, World Lifestyle Medicine Education Services (WLMES); Vice President, International Society of Digital Medicine (ISDM); Director, IORMA Futures Health and Wellbeing Technology Centre; CEO & Founder, 360in360 Immersive Experiences
Department: Not applicable (leadership roles across organizations)
Organization: Multiple (WLMES, ISDM, IORMA, 360in360)
Country: United Kingdom

Dr. Nilesh Charankar

Role: Lead Full-Stack Developer / Researcher / Author
Department: Technology / Software Engineering focus
University: industry professional
Country: India

Dr. Sai Suman Singamsetty

Role: Data Management Specialist / Keynote Speaker / Independent Researcher
Department: Electronics & Communication Engineering
University: Centurion University of Technology and Management
Country: India

Dr. Maria Cecilia Colautti

Role: Secretary, ICOH Scientific Committee on Nanomaterial Workers’ Health
Department: Occupational Health / Nanotechnology (Faculty of Engineering)
University: Universidad Nacional de la Patagonia San Juan Bosco (UNPSJB)
Country: Argentina

Dr. Manjunath G N

Role: Professor & Head of Department
Department: Pharmacology, Sri Siddhartha Medical College
University: Sri Siddhartha Academy of Higher Education
Country: India

Prof. Heba Afify

Role: Professor / Associate Professor
Department: Biomedical Engineering
University: Cairo University (PhD); Shorouk Academy / MTI University (current affiliations)
Country: Egypt

Dr. Ju Lee Kim

Role: Senior Researcher.
Department/Organization: R&D Center, RedGene.
University (Academic Background): Westfälische Wilhelms-Universität Münster
Country: Republic of Korea

Overview:

This conference gathers industry leaders, researchers, clinicians, regulators, and technology developers to discuss innovations in medical devices along with regulatory science and compliance. The focus lies on advances in device technologies, clinical validation, regulatory frameworks, quality assurance, digital health integration, and pathways to market approval to enhance patient safety and healthcare outcomes.

Structure and Sessions (Who Does What):

Organizing Committee: Manages program design, abstracts peer review, speaker invitations, and event logistics.
Keynote Speakers: Influential experts provide plenary talks on emerging device technologies, regulatory updates, and quality standards.
Session Chairs: Moderate technical and regulatory sessions, facilitate panel discussions, and lead Q&A.
Presenters: Engineers, clinicians, regulatory professionals, and researchers present scientific papers, case studies, and policy perspectives.
Participants: Engage in workshops, poster presentations, and networking sessions to share knowledge and build collaborations.
Peer Review Committee: Ensures double-blind peer review of submissions to maintain academic and industry standards.

Participate and Contribute (Who Benefits):

Medical Device Engineers & Developers: Learn about latest innovations and regulatory requirements.
Regulatory Affairs & Compliance Professionals: Gain insights into evolving regulations and quality management systems.
Clinicians & Healthcare Providers: Understand clinical implications and technological advancements.
Industry & Business Leaders: Explore commercialization strategies, market trends, and partnership opportunities.
Students & Early Career Researchers: Present research, network, and enhance knowledge.

Benefits:

Certificate of Participation / Presentation
Get DOI (Crossref) for your abstract
CPD Certificate
Opportunity to Become a Keynote Speaker
Free Access to 170+ Millions of Metadata Records
Abstract Indexed in Google Scholar & 10+Indexing

Abstract Topics / CFP (Call for Papers) Tracks:

Medical Device Innovation & Emerging Technologies
Clinical Trial Design & Device Validation
Regulatory Science and Compliance Updates
Quality Assurance & Risk Management
Digital Health, Software & Connected Devices
Human Factors & Usability Engineering
Medical Device Market Access & Reimbursement
Legal and Ethical Considerations in Medical Devices
Artificial Intelligence in Medical Devices
Manufacturing & Supply Chain Excellence
Post-Market Surveillance & Real-World Evidence
Global Harmonization & Regulatory Pathways

Detailed Program Grid (2 Half Days – 8 AM to 12 PM IST)

Time	Day 1	Day 2
08:00–08:15	Opening Ceremony & Welcome Address	Recap of Day 1 & Opening Keynote
08:15–09:00	Keynote I: Innovations in Medical Device Technologies	Keynote III: Regulatory Trends & Quality Management
09:00–09:45	Technical Session I: Device Validation & Clinical Trials	Technical Session III: AI & Software as Medical Devices
09:45–10:00	Q&A and Networking Break	Q&A and Networking Break
10:00–10:45	Technical Session II: Digital Health & Connected Devices	Panel Discussion: Global Regulatory Harmonization
10:45–11:30	Abstract Presentations & Case Studies	Technical Session IV: Post-Market Surveillance & Safety
11:30–12:00	Participant Feedback & Closing Remarks	Closing Ceremony & Certificate Distribution

Submit Abstract & Registration

Conference Dates	Conference Title	Timing (IST)	Abstract Submission Deadline	Registration Deadline
17th, 18th June 2026	IVC on Medical Devices, Innovation & Regulation	8:00 AM – 12:00 PM	8th June 2026	10th June 2026

Abstract Guidelines:

300–350 words including Title, Author(s), Affiliation, Email, and 5 Keywords
Font: Times New Roman, 12 pt, 1.5 spacing
File Format: .doc or .docx only
Peer review through double-blind evaluation

Conclusion:

The International Conference on Medical Devices, Technologies & Regulation provides a vital forum for interdisciplinary knowledge exchange, advancing innovation while ensuring regulatory compliance and patient safety in the medical device sector.

Registration

Type of participation

Early Bird Registration

May 13, 2026

Mid Registration Deadline

May 27, 2026

Late Registration Deadline

June 10, 2026

No. of Participants ($159 each under Speaker / Poster (Virtual)) :

No of Accompanying Persons ($ 200 each )

Registration Summary

Registration Price (Per Person - Speaker / Poster (Virtual)):

$159

Participants:

Total Registration Price:

$159

Total Price:

$159

By clicking "Proceed to Pay", you agree to the privacy policy, terms & conditions and cancellation policy.

Note: For more information on registration queries, please contact: support@onegrasp.com

Registration includes:

For In-person attendees

Entry to all conference sessions, poster presentations, and the exhibition area
Conference kit comprising a name tag, program booklet, and abstract book
Two coffee breaks and lunch are provided for each day of the conference
Accreditation Certificate issued by the Organizing Committee

For Virtual Attendees

This category enables participants to present virtually at the conference from the convenience of their home or workplace without the need for in-person attendance. It includes:

Access to all presentations
An E-abstract book and program
An E-certificate for presentation and participation
A CPD (Continuous Professional Development) Certificate with Credits

Terms and Conditions

By enrolling in the conference, you hereby express your acceptance of the terms and conditions stated herewith.

The organization retains the authority to modify the program, date, and/or location at its discretion, without prior notification.

The organization cannot be held accountable for any loss or damage incurred due to substitutions, adjustments, delays, or cancellations of an event caused by unforeseen factors beyond its control. Such factors encompass, but are not limited to, force majeure, natural disasters, acts of sabotage, accidents, labor disputes, acts of terrorism, strikes, or hostilities.

The organization reserves the right and possesses the exclusive discretion to cancel any conference at any time under circumstances that are unavoidable and unanticipated. The organizer will not assume any additional liability towards the participant.

Registrations will remain valid for rescheduled events or future editions if the conference must be postponed due to circumstances beyond the organizer's control. Refund policies do not apply under these conditions.

In the instance of cancellation, the organization will make reasonable and appropriate alternative arrangements, which may include posting the cancellation notice on the relevant event website to inform those who have secured bookings or purchased tickets for the event.

Attendees are responsible for reviewing this information before the event. We strongly recommend regularly checking the conference website for updates.

The organizers shall not be held responsible for personal injuries or for the loss or damage to personal belongings of attendees, either during the conference.

Important COVID-19 Update for Participants

In case of any natural calamities, those who are unable to attend in person due to travel restrictions or health concerns, enable your virtual participation. Details on accessing the virtual platform will be provided 2 months prior to the conference. And on your request the registration will transfer to future editions.

We will provide regular updates on the conference website regarding any changes to the event format, health and safety measures, and other relevant information. Please check the website periodically for the latest updates.