Meet Accuprec Research Labs at MEDICA 2026
Messe Düsseldorf, Düsseldorf, Germany | Hall 16, Stall C35-1
16–19 November 2026
Accuprec at MEDICA 2026
Accuprec Research Labs Pvt. Ltd. is pleased to participate in MEDICA 2026, one of the world’s leading exhibitions for the medical technology and healthcare industry. Join us in Düsseldorf, Germany, to explore comprehensive medical device testing solutions, discuss your technical requirements and connect with our team about your upcoming projects.
As a globally reputed Contract Research Organization (CRO) for pharmaceutical and medical device testing, Accuprec Research Labs supports manufacturers with scientific testing, product evaluation and regulatory-focused services designed to help address the quality, safety and performance requirements of medical devices.
We look forward to meeting medical device manufacturers, healthcare innovators, biotechnology companies, regulatory professionals and industry partners from around the world.
Dates
16–19 November 2026
Venue
Messe Düsseldorf, Düsseldorf, Germany
Find Us
Hall 16 | Stall C35-1
Schedule a Meeting
Write to us at info@accuprec.com
Planning your visit to MEDICA 2026?
Book a one-on-one meeting with our scientific experts at Hall 16, Stall C35-1.
Meet Our Directors
Connect with the Accuprec Research Labs team at MEDICA 2026 to discuss your medical device testing challenges, project requirements, regulatory considerations and potential collaborations.
Dr. Manish Rachchh
Director & CEO
Dr. Manish Rachchh represents Accuprec Research Labs’ leadership in delivering scientific testing and research solutions for the pharmaceutical and medical device industries. Meet him to discuss organizational capabilities, strategic partnerships and your broader testing requirements.
Mr. Mayur Kandoriya
Director & CMO
Mr. Mayur Kandoriya works with industry partners to explore business collaborations and understand their testing needs. Connect with him to discuss potential partnerships, project enquiries and how Accuprec’s testing capabilities may align with your business requirements.
Dr. Jainik Khamar
Assistant Manager (PT)
Connect with Dr. Jainik Khamar to discuss project-related enquiries and medical device testing requirements. Our team looks forward to understanding your technical needs and identifying relevant testing support for your products.
Comprehensive Medical Device Testing Services
Accuprec Research Labs offers a broad range of medical device testing and evaluation services to support manufacturers throughout product development, quality assessment and regulatory preparation. Our capabilities are designed to help address material safety, product integrity, microbiological quality and performance-related requirements.
Biocompatibility Testing
Biocompatibility testing is an important component of medical device biological evaluation. It helps assess potential biological risks associated with device materials and their intended contact with the human body.
Our biocompatibility testing services support the evaluation of medical devices and relevant materials based on their intended use, nature of body contact and duration of exposure.
View ServiceServices may support:
- Biological evaluation of medical device materials
- Assessment of potential biological responses
- Testing strategies based on the device’s intended application
- Scientific data generation to support biological safety evaluations
- Testing requirements aligned with applicable standards and regulatory expectations
Extractables, Leachables & Toxicological Risk Assessment (TRA)
Extractables and leachables studies help identify and characterize chemical substances that may originate from medical device materials, components and packaging systems.
Extractables studies investigate compounds that may be released under defined laboratory extraction conditions, while leachables assessments focus on substances that migrate under relevant conditions of use or storage.
View ServiceOur service offering includes:
- Extractables profiling
- Leachables identification and assessment
- Chemical characterization of detected compounds
- Evaluation of unknown compounds, where applicable
- Toxicological Risk Assessment (TRA) support
- Analytical method development and validation, as required
- Scientific reporting to support product safety assessments and regulatory documentation
Stability & Transportation Testing
Medical devices and their packaging systems may be exposed to different environmental and transportation conditions throughout their lifecycle. Stability and transportation testing helps assess whether specified product characteristics remain acceptable under defined conditions.
View ServiceOur testing support can help manufacturers evaluate:
- Product stability under specified storage conditions
- The effects of defined environmental exposures
- Product and packaging integrity following transportation simulation, where applicable
- Changes in relevant physical or functional characteristics
- Data requirements for shelf-life and product lifecycle assessments
Packaging & Mechanical Testing
Medical device packaging plays an important role in protecting products during storage, handling and transportation. Mechanical testing helps assess relevant physical properties and performance characteristics of devices, components and packaging systems.
View ServiceOur packaging and mechanical testing support may include:
- Assessment of packaging integrity
- Evaluation of relevant physical and mechanical properties
- Testing of device components under defined conditions
- Evaluation of packaging performance during handling and transportation
- Generation of test data to support product quality and performance assessments
Microbiological Testing
Microbiological testing supports the evaluation of relevant microbiological quality and safety characteristics of medical devices and associated materials.
View ServiceDepending on the product and study requirements, testing may support:
- Microbiological quality assessment
- Evaluation of microbial contamination
- Relevant microbiological testing of medical devices and materials
- Generation of scientific data for quality and safety evaluations
- Support for applicable microbiological testing requirements
Clinical Evaluation
Clinical evaluation is an essential part of demonstrating the safety and performance of medical devices in their intended use. It involves the systematic assessment of relevant clinical evidence in accordance with applicable regulatory requirements.
View ServiceOur clinical evaluation support can help manufacturers with:
- Review and assessment of relevant clinical evidence
- Evaluation of available clinical data
- Assessment of safety and performance information
- Identification of relevant evidence gaps
- Preparation and organization of clinical evaluation documentation
- Support for regulatory-focused clinical evidence assessments
Why Choose Accuprec?
Accuprec Research Labs is committed to supporting the scientific and testing needs of pharmaceutical and medical device organizations through comprehensive laboratory capabilities and a quality-focused approach.
Comprehensive Testing Capabilities
Multiple testing services to address different medical device development and evaluation requirements.
Scientific Expertise
A team focused on understanding product-specific testing challenges.
Regulatory-Focused Support
Testing and documentation support aligned with applicable standards and study requirements.
Collaborative Approach
Engagement with manufacturers to understand project objectives and identify suitable testing strategies.
Commitment to Quality
A focus on accurate testing, reliable reporting and scientifically supported results.
