Pioneering advancements in dermatological clinical research
Dermatological issues stand as some of the most prevalent medical concerns, encompassing both typical ailments like acne, atopic dermatitis, psoriasis, and hair loss, as well as rarer skin conditions. For those at the forefront of innovative practices within dermatology, we extend comprehensive clinical development and therapeutic proficiency in the realm of dermatology medical device advancement.
Trust in the seamless design and execution of your dermatology trial, under the tutelage of our cross-functional team of medical, operational, regulatory, and imaging experts. At Eclevar, we are committed to propelling the field of dermatology forward through excellence in research and practice.
With offices in Europe, the United Kingdom, and Australia, we have the capability to conduct international multi-site clinical trials while providing local support to our clients.
CRO services for Dermatology Medical Device
At Eclevar, we specialize in orchestrating groundbreaking clinical trials for medical devices tailored to dermatology.
- Development of protocol and other study documents
- Identification of clinical trial sites and investigators
- Training, startup, and management of clinical sites
- Communication between research teams
- Identification of project risks
- Quality management
Trial closeout and reporting
From concept to execution, our end-to-end solutions encompass every aspect of dermatology medical device trials. Whether you’re introducing a novel diagnostic tool, a revolutionary treatment modality, or an innovative monitoring device, Eclevar have the expertise to guide you through the entire journey.
Reliable Site Selection for Clinical Trials
To ensure the success of a clinical trial, our team work to optimize Site Selection by employing best practices for early site feasibility analysis and fostering of strong partnerships.
Early Site Feasibility Analysis: a thorough assessment of the potential site’s geography, population profiles, study design, ethical considerations, study timelines, and existing partnerships/competitors.
- Population Profiles: understanding of the demographics and characteristics of the patient population.
- Partnerships and Staffing: collaboration with medical and social community members.
CRO Site Management
Eclevar has more than 20 years of experience in providing modern solutions for the medical industry. Our site management services are designed to streamline your clinical trial operations ensuring compliance with protocols, regulatory guidelines, and Good Clinical Practice standards.
- Documentation
- Regulatory approvals
- Monitoring the outgoing trial
- Patient recruitment
- Staff recruitment and training
- Investigators and sub-investigators.
- Institutional Review Boards (IRB) submissions.
Accurate PMCF Data Collection in demartology
Our PMCF Data Collection activities helps manufacturers gain valuable insights into the real-world use of their products and make informed decisions to enhance patient safety and product effectiveness.
- Randomised control trials
- Prospective controlled study
- Retrospective study
- Systematic review
- Observational studies
- Registry studies
Eclevar has a team of experienced professionals ready to assess the benefit/risk ratio throughout the product’s lifespan.
Work alongside Eclevar for study design and patient recruitment
Contact us today to embark on a journey of innovation and collaboration in the meticulous planning and execution of your upcoming dermatology clinical trial.
