Medical Device Regulatory Services

��ϲ��’s regulatory advisors have 30 years of domestic and international medical device regulatory consulting experience, specializing in handling the most complex challenges and partnering with you on the path to submission.

Our approach to medical device regulatory consulting

��ϲ�� offers a unique approach to assist from early stage design through commercialization. ��ϲ��’s multidisciplinary team of experts has a deep understanding of the medical device product life cycle, and the impact certain decisions can have on regulatory success.

��ϲ�� offers a talented team with a wide range of expertise that is ready to support your goals. With 16 laboratories in our life sciences division to help support your projects, you can leverage a one-stop-shop for all of your project needs.

The ��ϲ�� advantage

Our advisors have worked with a multitude of clients, including some of the world’s largest medical device manufacturers, and will ensure you are receiving the proper guidance for all stages of product development and commercialization goals. Trusting the right partner for your business is critical and ��ϲ��’s position in the medical device industry across multiple segments, helps drive the certainty of a successful submission.

Comparative Analyses

��ϲ�� utilizes a proprietary methodology to help streamline non-clinical testing and support all marketing applications. The proprietary methodology combined with our extensive biomechanical and physiological knowledge has been successfully implemented for over 10 years.

Design Assessment

With 30 years of experience on a diverse range of products, ��ϲ�� can help you make the best design decisions to ensure the optimal performance and safety of your product.

Risk Analysis and Mitigation

Our experts will help you perform a comprehensive risk assessment and create mitigation activities to ensure regulatory success.

Strategic Test Plans and Regulatory Pathway

��ϲ��’s experts will provide thorough test strategies that align with your regulatory goals.

Pre-clinical Evaluations

Our regulatory and consulting team can provide regulatory and pre-clinical testing strategies to outline all the testing needed to support your goals.

Clinical Evaluation Reports (CERs)

Our regulatory team is well-versed in the Medical Device Regulations (MDR) and can author full CERs and literature reports.

Project Management

The regulatory landscape can be difficult to navigate, ��ϲ�� offers support to manage your pathway to market from design support through clearance/approval.

FDA Submissions and Reports

Our regulatory team will provide the highest quality FDA submissions. ��ϲ�� has experience with some of the most complex submissions and will ensure you are receiving the best support throughout the regulatory submission process. Our submission support includes but is not limited to:

510(k)s
Pre-Submissions / Q-submissions
Investigational Device Exemption (IDE)
Humanitarian Device Exemption (HDE)
Emergency Use Authorization (EUA)
Breakthrough device designation
Safer Technologies Program (STeP)
De Novos

Deficiency Response Strategies and Support

Receiving an FDA deficiency notice and the way you respond is critical to obtaining clearance and addressing FDA concerns. Using our collaborative approach, ��ϲ�� can help facilitate conversations and leverage our established brand to work through the deficiencies.

Medical Device Regulatory Affairs

Additional Medical Device Services

In addition to medical device regulatory guidance, we provide testing and certification services for a wide variety of medical devices and products.

Some of our testing services include:

Making certain for nearly 190 years

Medical Device Testing

As a comprehensive testing partner, you’ll enjoy the benefit of a single supplier source for all of your testing needs, from mechanical testing and environmental simulation to EMC and wireless device testing.

EMI & EMC Testing

��ϲ�� performs electromagnetic compatibility (EMC) and electromagnetic interference (EMI) testing for a variety of medical devices and components, including implantable devices, diagnostic tools and therapeutic equipment.

Medical Device Battery Testing

��ϲ�� provides safety and certification testing for rechargeable lithium-ion and nickel metal hydride batteries used in hospital and home health applications.

Orthopedic Implant Testing

As a global leader in orthopedic implant testing, ��ϲ�� has years of experience in evaluating hip replacements, knee prostheses, spinal devices and many other implants.

Our team of over 9,000 Engaged Experts in North America, Europe, The Middle East, Australia, Asia and Africa are ready to help you.

Make an inquiry today

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