Exhibition Announcement

Meet Accuprec at KIMES 2026

Accuprec Research Labs Pvt. Ltd. is proud to participate in KIMES 2026, one of the largest global exhibitions for medical and healthcare technologies.

We invite medical device manufacturers, pharmaceutical companies, and healthcare innovators to visit our stall and explore our advanced testing and regulatory support services.

19th – 22nd March 2026
COEX, Seoul, South Korea
Stall No: D-817

With internationally recognized accreditations and a highly experienced team, Accuprec helps organizations ensure product safety, regulatory compliance, and global market readiness.

Meet our experts to discuss how our testing solutions can support your product development, validation, and international regulatory approvals.

Expert Seminar at KIMES 2026

Accuprec will host an Expert Seminar on the latest regulatory developments in medical device biocompatibility testing. The session will highlight ISO 10993-1:2025 updates and regulatory strategies for global compliance.

Seminar Topic
Regulatory Requirements & Strategy
Standard
ISO 10993-1:2025
Date
March 20, 2026
Venue
COEX, Seoul – 3F, Room 325
Key Highlights
  • Latest updates in ISO 10993-1:2025
  • Regulatory expectations for biological evaluation
  • Risk-based compliance strategies for medical devices
  • Toxicological risk assessment insights
Seminar Schedule
Session 1
Biocompatibility Testing
🕥 10:40 – 11:40
Session 2
Extractables & Leachables
🕑 14:40 – 15:40
Speaker
Dr. Manish Rachchh
Director & CEO – Accuprec Research Labs Pvt. Ltd.
Expert in biocompatibility testing and regulatory strategy for medical device compliance.
Our Testing Services

Accuprec provides comprehensive testing and regulatory solutions for pharmaceutical and medical device industries in accordance with international standards.

Biocompatibility Testing

Biocompatibility testing evaluates the biological safety of medical devices when they come into contact with the human body. Our testing helps ensure that materials used in medical devices do not cause toxicity, irritation, or adverse biological reactions.

ISO 10993-1:2025

Packaging & Mechanical Testing

We evaluate the strength, durability, and integrity of medical device packaging systems to ensure products remain sterile and protected throughout storage, transportation, and handling.

ISO 11607-1 & ISO 11607-2

Extractables, Leachables & Toxicological Risk Assessment

Our advanced analytical studies identify chemical substances that may migrate from materials or packaging into medical products. We also perform toxicological risk assessments to ensure patient safety and regulatory compliance.

ISO 10993-18 & ISO 10993-17

Clinical Evaluation Report – CER

Accuprec supports manufacturers with comprehensive Clinical Evaluation Reports required for regulatory approvals. Our experts analyze clinical data and scientific literature to demonstrate the safety and performance of medical devices.

ISO 14155

Stability & Transportation Testing

These studies simulate real-world storage and transportation conditions to verify product stability, packaging integrity, and shelf life under various environmental conditions.

ASTM F1980 & ASTM D4169

Microbiological Testing

We provide microbiological testing to assess bioburden, sterility, and microbial contamination levels in medical devices and pharmaceutical products to ensure compliance with international standards.

ISO 11737-1, ISO 11737-2 & USP
Meet Our Team at KIMES

Our leadership team will be present at the exhibition to discuss your testing requirements and regulatory challenges.

Dr. Manish Rachchh

Director & CEO
📞 +91 90999 81023

Mr. Mayur Kandoriya

Director & CMO
📞 +91 99099 19545

Mr. Jainik Khamar

Assistant Manager (PT)
📞 +91 90999 32948

Contact Us

If you would like to schedule a meeting during KIMES 2026 or learn more about our services, please contact us.

✉️ info@accuprec.com
📞 +91 90996 16769
📞 +91 90999 81023
📞 +91 99099 19545
🌐 www.accuprec.com

Visit Accuprec Research Labs Pvt. Ltd. at Stall D-817 and discover how our testing expertise can help accelerate your path to global compliance.