Visit Accuprec at MEDICA 2025

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

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

Services

1. Biocompatibility Testing of Medical Devices

Ensuring biological safety for every device (ISO 10993 series, USFDA 21 CFR).

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2. Extractable / Leachable & TRA Testing

Identifying and managing chemical risks; ISO 10993-18/-17 compliance.

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3. Stability & Transportation Testing

Real-time, accelerated & transit simulation testing (ASTM, ISTA, ICH).

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4. Packaging & Mechanical Testing

ISO 11607 validation, seal strength, sterilant penetration, aging & durability.

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5. Clinical Evaluation Report (CER)

MDR 2017/745, MEDDEV 2.7/1 Rev. 4, Annex XIV — regulator-ready CERs.

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6. Microbiological Testing

Bioburden, sterility, endotoxin, PET, EM programs; ISO/USP/WHO compliant.

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Meet Us at MEDICA 2025

Hall No. 16 / C35-2 — 17–20 November 2025, Düsseldorf, Germany

Write to us: info@accuprec.com