Accelerate Cosmetics & Skincare Clinical Research Through Connected Workflows

Support cosmetics and skincare studies through connected clinical workflows designed to streamline participant engagement, data collection, scheduling, and decentralized trial execution.

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Problem

We Understand the Unique Needs of Dermatology, Cosmetics, & Skincare Clinical Trials

01 Participant Recruitment and Diversity

Support broader and more diverse participant recruitment through connected engagement and decentralized participation workflows.

04 Integrated Real-time Data Management

Access centralized and connected data workflows that simplify coordination and operational visibility across clinical studies.

02 Skin Health Monitoring

Enable real-time skin health monitoring through connected assessments, photo capture workflows, and remote participant participation.

05 Sensitive Data Security

Maintain secure clinical workflows and protected participant data across decentralized and hybrid study environments.

03 Protocol Compliance

Support participant adherence through automated scheduling, reminders, and connected engagement workflows.

06 Regulatory Compliance

Support compliant clinical trial execution through centralized documentation, tracking, and operational workflows.

Problem

We Understand the Unique Needs of Dermatology, Cosmetics, & Skincare Clinical Trials

01 Participant Recruitment and Diversity

Support broader and more diverse participant recruitment through connected engagement and decentralized participation workflows.

03 Protocol Compliance

Support participant adherence through automated scheduling, reminders, and connected engagement workflows.

05 Sensitive Data Security

Maintain secure clinical workflows and protected participant data across decentralized and hybrid study environments.

02 Skin Health Monitoring

Enable real-time skin health monitoring through connected assessments, photo capture workflows, and remote participant participation.

04 Integrated Real-time Data Management

Access centralized and connected data workflows that simplify coordination and operational visibility across clinical studies.

06 Regulatory Compliance

Support compliant clinical trial execution through centralized documentation, tracking, and operational workflows.

Problem

We Understand the Unique Needs of Dermatology, Cosmetics, & Skincare Clinical Trials

01 Participant Recruitment and Diversity

Support broader and more diverse participant recruitment through connected engagement and decentralized participation workflows.

02 Skin Health Monitoring

Enable real-time skin health monitoring through connected assessments, photo capture workflows, and remote participant participation.

03 Protocol Compliance

Support participant adherence through automated scheduling, reminders, and connected engagement workflows.

04 Integrated Real-time Data Management

Access centralized and connected data workflows that simplify coordination and operational visibility across clinical studies.

05 Sensitive Data Security

Maintain secure clinical workflows and protected participant data across decentralized and hybrid study environments.

06 Regulatory Compliance

Support compliant clinical trial execution through centralized documentation, tracking, and operational workflows.

Patient Journey for Cosmetics & Skincare Clinical Research

Solutions

Our Solutions for Cosmetics & Skincare Clinical Research

Unified Clinical Study Access

Accelerated Recruitment

Access connected clinical workflows through one centralized environment designed to support cosmetics and skincare studies efficiently.

Reduced Manual and Repetitive Tasks

Flexible & Accessible Participation

Automate repetitive workflows, participant follow-ups, and operational coordination to reduce administrative burden across study execution.

Reduced Communication Burden

Flexible Study Configuration

Streamline participant and study team communication through connected messaging, reminders, and engagement workflows.

Accelerated Time to First Patient First Visit (FPFV)

Improve Retention & Participant Engagement

Simplify study setup and participant engagement workflows to accelerate time to first patient first visit across clinical studies.

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Jeeva Benefits

Launch cosmetics and skincare clinical studies in less than four weeks

Up to 2X faster to first patient first visit (FPFV) while reducing operational costs

Reduce logistical burden on study teams by over 70%

Access connected workflows securely across browser-based devices

Real-time centralized monitoring and operational visibility

Premium 24/7 study support for research teams

Connect with sites and participants through multilingual engagement workflows

Clients Love Jeeva Solutions

Compliance Programs Supported 

Testimonials

Client Testimonials

We unified our clinical research workflows enterprise-wide using Jeeva, enabling our small team to efficiently manage all studies with highly responsive support. We are saving 60% time effort across all clinical trials.

Luma Melo, PhD, MSc, MBA, MA

Taxa technologies

Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.

Marshall Summar, MD, Ph.D

CEO, Uncommon Cures LLC

Jeeva is backed by excellent customer service. We are enjoying our seamless transition to this platform for our longitudinal cohort study. Flexibility in programming.

Dr. Lawrence Cheskin, MD

Professor and Chair, Nutrition and Food Studies, George Mason University

We are thrilled to partner with Jeeva to bring next-generation efficiencies to clinical research. The need for AI-driven automation in clinical trials has never been greater, and a unified CTMS approach is exactly what the industry needs

Gurudath Gurjal, MSc

Director, ClinTrek

Luma Melo, PhD, MSc, MBA, MA

Taxa technologies

Marshall Summar, MD, Ph.D

CEO, Uncommon Cures LLC

Jeeva is backed by excellent customer service. We are enjoying our seamless transition to this platform for our longitudinal cohort study. Flexibility in programming.