Accelerate Your Medical Device Testing & Regulatory Submissions
Join us at MEDICA 2025 to explore how Accuprec can help accelerate your medical device testing, validation and regulatory submissions.
📍 Hall No. 16 / C35-2 | 📅 17–20 November 2025 | Düsseldorf, Germany • 📧 info@accuprec.com • 🌐 www.accuprec.com
Globally Reputed CRO for Medical Device Testing
Accuprec Research Labs is a globally recognized Contract Research Organization (CRO) specializing in end-to-end testing, validation and regulatory support for medical devices. Accredited by ISO/IEC 17025, OECD GLP, AAALAC and recognized by global regulatory agencies including USFDA, EMA and ASCA-A2LA, we ensure that every medical device we evaluate meets the highest standards of safety, quality and performance.
With a 1,20,000 sq. ft. state-of-the-art facility, 250+ qualified scientists and operations spanning 13 specialized testing verticals, we serve as an extended R&D and regulatory partner for 1,000+ global manufacturers. Meet our expert team at MEDICA 2025 and discover how Accuprec supports you from concept to clinical validation and market launch.
Why Visit Us at MEDICA 2025?
- Learn how Accuprec’s scientific expertise can accelerate your medical device approval process.
- Discuss your testing and validation needs directly with our leadership team.
- Explore potential collaborations and partnerships for global regulatory submissions.
- Experience our commitment to innovation, precision, and quality assurance.
Meet Our Team in Düsseldorf



Services
1. Biocompatibility Testing of Medical Devices
Ensuring biological safety for every device (ISO 10993 series, USFDA 21 CFR).
Read More2. Extractable / Leachable & TRA Testing
Identifying and managing chemical risks; ISO 10993-18/-17 compliance.
Read More3. Stability & Transportation Testing
Real-time, accelerated & transit simulation testing (ASTM, ISTA, ICH).
Read More4. Packaging & Mechanical Testing
ISO 11607 validation, seal strength, sterilant penetration, aging & durability.
Read More5. Clinical Evaluation Report (CER)
MDR 2017/745, MEDDEV 2.7/1 Rev. 4, Annex XIV — regulator-ready CERs.
Read More6. Microbiological Testing
Bioburden, sterility, endotoxin, PET, EM programs; ISO/USP/WHO compliant.
Read MoreMeet Us at MEDICA 2025
Hall No. 16 / C35-2 — 17–20 November 2025, Düsseldorf, Germany