Meet Accuprec at WHIF 2025
Complete Medical Device Testing Under One Roof
Complete Medical Device Testing Under One Roof
The global medical device industry is expanding rapidly and with it comes the need for stronger safety, quality and regulatory compliance. Accuprec Research Labs is proud to participate in the World Health Innovation Forum (WHIF) 2025 to support manufacturers with simplified testing, validation and documentation for global approvals.
Location: Stall C-14
Dates: December 11–13, 2025
Venue: AMTZ, Visakhapatnam
What’s New at WHIF 2025
Accuprec is now working with the revised ISO 10993-1:2025 framework, which introduces a stronger risk-based approach for biological evaluation.
This update helps manufacturers reduce unnecessary studies and bring more clarity to device safety requirements.
At WHIF 2025, our team will walk visitors through how the updated standard supports:
- ➥ Better biological evaluation planning
- ➥ Smarter study selection
- ➥ Less duplication and re-testing
- ➥ Faster and smoother regulatory submissions
Accuprec at WHIF 2025
Accuprec is one of India’s most trusted partners in regulatory testing and documentation. At WHIF 2025, our team will demonstrate how complete device testing under one roof ensures:
- Faster approvals
- Reduced regulatory risk
- Accurate and reliable data
- Compliance with global standards such as USFDA, EU MDR, CDSCO and more
Our Key Services Showcased at WHIF
1. Biocompatibility Testing (ISO 10993-1:2025)
Risk-based evaluation
Biological evaluation planning
Minimizing duplication and re-testing
2. Extractables, Leachables & Toxicological Risk Assessment
ISO 10993-17/18 compliant
Hidden chemical risk evaluation
Support for regulatory acceptance
3. Stability & Transportation Testing
Real-time and accelerated stability studies
ISTA/ASTM transport simulation
Shelf-life evaluation
4. Packaging & Mechanical Testing
ISO 11607 packaging validation
Mechanical and material performance testing
Sterility and protection assurance
5. Clinical Evaluation Reports (CER)
EU MDR 2017/745 compliant
Literature review, PMS, PMCF
Risk management integration
6. Microbiological Testing
Sterility and bioburden
Endotoxin testing
Environmental monitoring
Why Meet Accuprec at WHIF?
- Faster approvals with all testing under one roof
- Reduced regulatory risk with globally aligned reports
- Accurate and reliable test data
- Updated guidance on new standards
- Single partner for all compliance needs
- Strong support for startups and innovators
Who Should Visit Us?
Ideal for:
- Medical device manufacturers
- R&D and QA teams
- Regulatory affairs professionals
- Startups and innovators
- Consultants and compliance partners
- Healthcare technology companies
Whether launching a new device or preparing for global approvals, our experts provide complete regulatory guidance.
Strengthening India’s Medical Device Ecosystem
Accuprec supports India’s mission to become a global manufacturing hub through:
- World-class laboratory infrastructure
- Comprehensive testing facilities
- Fast turnaround times
- Expert regulatory guidance
- Reliable data for global submissions
WHIF 2025 offers an excellent opportunity to understand how Accuprec can support your compliance journey.
Visit Accuprec at WHIF 2025
Dates: December 11–13, 2025
Venue: AMTZ, Visakhapatnam
Stall: C-14
Visit Accuprec at WHIF 2025 — Stall C-14
Meet our experts and discuss how we can support your product’s regulatory journey.
Book a Meeting