Clinical Services
Transforming a new drug or medical device technology into a treatment opportunity is a complex, expensive, and time-sensitive process. We can help you navigate the clinical development process through all clinical phases.
Service Offerings
Our team has extensive clinical development experience, and we offer a full range of services across all phases of drug and medical device development. From regulatory affairs to clinical trials and market access for commercialization, we have the expertise and experience to help you succeed.
Our clinical service offerings include:
- Early phase benchmarking and characterization
- Identify suitable endpoints and study designs
- Study planning and early concept development and design
- Scientific assumptions, preclinical data, risk mapping and market opportunity
- Clinical study competitive landscape
- Feasibility assessment and return on investment of clinical trial concepts
- Physician and patient feasibility assessments
- Bridging study characterization to support reference and historical data
- Patient mapping
- Patient advocacy planning
- Scientific and medical advisory boards
- Risk assessment and mitigation
- REMS program planning and consultation
QNova LifeSciences has partnered with leading clinical research organizations (CROs) to support clinical studies worldwide, regardless of clinical phase. Our strategic partners are able to provide an integrated solution that is tailored to meet our client needs. Meet our clinical CRO partners who have the proven ability to execute your study.
- Tigermed USA
- CMIC Group
- Validcare
- Meditip
- New Day Diagnostics
Contact us today to learn more about how our clinical services can support the development of your product.
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Accelerate timelines and reduce risks.
By bringing the relevant expertise to clinical trial design, planning, and execution, we remove barriers to patient participation, accelerate timelines, and reduce risk.
Strategy and Planning
Each milestone of development has a timeline and cost used to map your business plan and to attract investment. Learn More
Study Documents
We have the experience and expertise to design and develop the clinical studies in accordance with the latest GCP and ICH guidelines.
Clinical Site Selection
We have a network of clinical sites that can align with your study objectives to accelerate study start-up.
Study Management
Our CRO partners have decades of experience in managing and monitoring clinical studies.
Advisory Board
Finding KOLs is challenging for small companies. Leverage our network to connect you with the relevant experts to best guide your technological and business development.