Service Providers
Name of Company
NEUROPHET Inc.
Address
12F, 124, Teheran-ro-, Gangnam-gu, Seoul, Republic of Korea
Key Services
  • Clinical CRO
  • Consulting
  • Decentralized Clinical Trial(DCT)
Homepage(English)
https://www.neurophet.com/en
Sales(end of 2024)
NR
Human Resources Status
NR
Number of audit of Regulatory agency(ex FDA/EMA, etc.)
NR
ISO 9001
Not Provided
Status of Additional Certifications
ISO 13485 (Medical Devices Quality Management System), ISO 27001 (Information Security Management), ISO 27701 (Privacy Information Management)
Key Strengths

Neurophet’s Imaging CRO strength lies in combining central imaging core lab operations, AI-powered neuroimaging analysis, regulatory-grade imaging workflows, and clinical trial execution support. Rather than functioning only as an imaging software provider, Neurophet can position itself as an end-to-end neuroimaging partner supporting sponsors from study design to imaging endpoint assessment. A key differentiator is Neurophet’s focus on neurology and neurodegenerative disease trials, particularly Alzheimer’s disease and related disorders. The company’s platform covers both MRI and PET modalities, supporting quantitative analysis of brain atrophy, white matter hyperintensity, amyloid/tau/FDG PET biomarkers, ARIA-related imaging findings, lesion tracking, and longitudinal disease progression. This allows sponsors to generate imaging-based evidence for patient selection, safety monitoring, efficacy evaluation, and regulatory decision-making.

Introduction Materials (Upload attachment)
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Services Provided by Clinical CROs
Clinical Operation
Provided
Medical Writing
Not Provided
Statistics
Not Provided
Data Management
Provided
Regulatory Affairs
Provided
Pharmacovigilance
Not Provided
Vendor Management
Provided
Consulting
Not Provided
Feasibility Service
Not Provided
Medical Monitoring
Not Provided
Training and Education
Provided
IT Solution
Not Provided
CDISC data service
Not Provided
Project Management
Provided
DCT Services (Decentralized Clinical Trials)
Online Subject Recruitment
Not Provided
E-Consent
Not Provided
IP (Investigational Product) Delivery
Not Provided
Remote Study (Remote Monitoring & Telemedicine)
Not Provided
In-home Research (Home Visits to the Subject’s Residence for Specimen Collection Including Blood Collection and Vital Sign Assessment)
Not Provided
Off-site Data Collection – Self-Collection of Specimens (e.g., Personal Diagnostic Kits)
Not Provided
Off-site Data Collection – Self-Measured Health Data (e.g., Personal Health Management Products, Wearable Devices, Medication Adherence Tools)
Not Provided
Cardiovascular Disease (CVD)
Not Provided
Diabetes / Endocrine Disorders
Not Provided
Respiratory Diseases
Not Provided
Sleep Disorders / Sleep Apnea
Not Provided
Obesity / Metabolic Syndrome
Not Provided
Medication Management (Electronic Pill Bottle, Recording Medication Intake, etc.)
Not Provided
Off-site data collection – self-report(ePRO/eCOA)
Not Provided
Remote Data Monitoring
Provided
Other
Consulting Services
Consulting
Provided