Business Details
11 Years
experience
Your Trusted Preclinical Research Partner for Medical Innovations
Since 2015, Surpass has been a leader in preclinical research, dedicated to advancing medical innovation through rigorous scientific testing. Our team of experts specializes in providing comprehensive preclinical services for medical devices, pharmaceuticals, biologics, and combination products, ensuring compliance with GLP standards. With state-of-the-art AAALAC-accredited facilities, we offer a full spectrum of testing services, including research models for dermal, gastrointestinal, neurological, and oncological applications. Our commitment to quality and innovation is driven by a proven comprehensive quality system, making us a trusted partner in the biomedical community.We support clients through every stage of product development, from feasibility studies to physician training, leveraging our expertise to translate research into life-saving solutions. Our remote study monitoring and downloadable white papers provide additional resources to enhance client collaboration. With a focus on excellence, Surpass continues to redefine the role of a preclinical contract research organization, delivering insights and support that propel medical advancements from concept to reality.
Services
Preclinical Testing
GLP Services
Research Models
Medical Device Testing
Pharmaceutical Testing
Details
- Year established: 2015
Highlights and features
- We operate AAALAC-accredited facilities for ethical and high-quality research.
- Our GLP-compliant services ensure regulatory compliance and data reliability.
- Award-winning team with expertise in diverse therapeutic areas.
- Full-spectrum preclinical support from feasibility to product development.
- Innovative approach combining scientific rigor with collaborative problem-solving.
Associations and certifications
- AAALAC
Services
Preclinical Testing
Surpass provides comprehensive preclinical testing for medical devices, pharmaceuticals, and biologics. Our services ensure regulatory compliance and data accuracy through GLP standards. Clients benefit from tailored study designs and expert analysis to advance innovations safely.
GLP Services
Our GLP-compliant services validate the safety and efficacy of medical products. With a proven quality system, we conduct rigorous studies that meet global regulatory requirements, ensuring reliable data for client submissions and development decisions.
Research Models
Surpass offers specialized research models for dermal, gastrointestinal, neurological, and oncological applications. These models enable precise testing of drug efficacy and safety, supporting targeted therapeutic development with translational relevance.
Medical Device Testing
We provide preclinical validation for medical devices, assessing performance and safety through customized protocols. Our expertise spans vascular, orthopedic, and urogenital devices, ensuring compliance with industry standards for market readiness.
Pharmaceutical Testing
Surpass conducts pharmaceutical testing for compounds like Alprazolam and Modafinil, evaluating pharmacokinetics and toxicity. Our studies support drug development pipelines with accurate data to inform clinical trial readiness and regulatory approval.
Questions
What services does Surpass offer?
Surpass provides preclinical testing for medical devices, pharmaceuticals, and biologics, including GLP services, research models, and product development support.
Are Surpass's facilities accredited?
Yes, Surpass operates AAALAC-accredited facilities, ensuring ethical and high-quality research standards.
What therapeutic areas do you specialize in?
We specialize in dermal, gastrointestinal, neurological, oncological, orthopedic, respiratory, urogenital, and vascular research models.
Do you support global regulatory compliance?
Yes, our GLP-compliant services meet international regulatory standards for data submission and product approval.
How can I access study resources?
Clients can download white papers and use MySurpass Remote Study Monitoring for real-time collaboration and data access.
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