• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trial Listings
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Directories » Research Center Profiles » International Dermatology Research, Inc.

AND
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • R
  • S
  • T
  • U
  • V
  • W

International Dermatology Research, Inc.

  • Profile
  • Contact Center or Provider

Profile

International Dermatology Research, Inc.

Contact Information

Contact: Silvia A. Trinidad
Phone: 305-225-0400
Fax: 305-227-0393
Email: Click here to see email.

Center Information

Silvia A. Trinidad
President/Research Director
International Dermatology Research, Inc.
8370 West Flagler, St. Suite 200
Miami, FL 33144
305-225-0400
Fax: 305-227-0393
strinidad@intldermresearch.com

Currently Enrolling Trials

    Show More

    Overview

    International Dermatology Research (IDR) is a privately owned research company and private practice specializing in dermatology. Established in 1993, it has successfully completed more than 600 clinical trials. Our staff is composed of two dermatologists, one nurse practitioner, two medical assistants, one aesthetician, two receptionists, one supervisor, three research coordinators, one general administrator/research director and three clinical research monitors.

    IDR also counts with 10 sites in Latin America, located in the following countries: Honduras (three sites), El Salvador (two sites), Panama (two sites) Dominican Republic (four sites) and Guatemala (one site). Most of our sites have more than 20 years of experience conducting clinical trials. All research staff is trained on GCP and ICH guidelines.

    Research Experience

    Our centers conduct phase II to IV studies, mainly in regular dermatology, but also in cosmetics and dermatology-related devices. In addition, three of our Latin American sites have the ability to conduct women's health studies. Among our clients are most major pharma as well as generics companies, and we can proudly state that several generic and brand-name medications have been FDA-approved based solely on the data provided by our centers. Furthermore, one of our sites in Honduras and one in the Dominican Republic have the capability to conduct phase I trials with vast experience in pediatrics PKs.

    Our research experience is comprised of the following therapeutic areas:

    • Acne
    • Actinic Keratosis
    • Alopecia
    • Atopic Dermatitis(Adults and Pediatrics)
    • Candidiasis
    • Cosmetics
    • Diaper Dermatitis
    • Eczema
    • Genital Warts
    • Hand Dermatitis
    • Hirsutism
    • Hyperhidrosis
    • Hypertrophic scars
    • Hidradenitis Suppurativa
    • Ichthyosis Vulgaris
    • Impetigo (over 4,500 cases conducted)
    • Keloids
    • Lamellar Ichthyosis
    • Lice Infestation
    • Melasma
    • Onychomycosis
    • Patch Testing
    • Palmoplantar Keratosis
    • Photoaging
    • Polymorphic Light Eruption
    • Psoriasis(Adults and Pediatrics)
    • Rosacea
    • Seborrheic Dermatitis
    • Scabies
    • Secondary Skin Infection
    • Solar Lentigines
    • Tinea Capitis
    • Tinea Corporis
    • Tinea Cruris
    • Tinea Pedis
    • Tinea Versicolor
    • Transdermal Devices
    • Urinary Tract Infection
    • Vulvo Vaginal Candidiasis
    • Vulvo Vaginal Atrophy
    • Warts

    Facility Description

    Our headquarters is located on one of Miami's main arteries, close to expressways and 10 minutes away from Miami International Airport and major hotel chains, such as Marriott, Hilton, Intercontinental, etc.

    The office features 5,500 square feet of space with 3,000 square feet dedicated to clinical research, 1,000 to regular dermatology practice and 1,500 to archiving. In addition, we have a CLIA-certified laboratory, set with -20º C and -70º C freezers for PK studies. Additionally, there are two fully customized monitoring areas with phones, internet connection, sound-proofed walls, refrigerator, coffee machine, copy/fax machine as well as an ample conference room equipped with TV.

    Investigator Experience

    Eduardo Weiss, MD

    Board-certified dermatologist
    Graduate Doctor of Medicine, Central University of Venezuela
    Dermatology Residency, Jackson Memorial Hospital
    Wound Healing Fellowship, University of Miami
    MOHs experience

    David Rodriguez MD
    Sub-investigator
    Dermatology Residency, University of Illinois
    Medical School University of Illinois Chicago
    Fellowship, Jackson Memorial Hospital

    Staff Expertise

    Silvia A. Trinidad
    President/Research Director
    40 years of experience in supervising clinical research and managing studies in the U.S. and Latin America

    Ariel F. Sotolongo, ARNP – Foreign MD
    Sub-investigator

    Efren Mendez, --Foreign MD
    Clinical Trial Manager

    Odett  Reina Suarez, Coordinator

    Mabel Canizares, Pharmacy Tech

    Delvis Jimenez, Foreign MD
    Clinical Research Coordinator

    Patient Demographics

    The patients population at our Miami headquarters office consists of White, Hispanic and African American patients and covers pediatrics to geriatrics. Patients in our database come mainly from Dade and Broward counties.

    Other Information

    Since we specialize mainly in dermatology, our staff has a vast experience in all dermatological- related conditions, giving us the ability to deliver very accurate data in a timely fashion. Furthermore, having 13 additional sites in Latin America allows us to facilitate fast enrollment with 95 percent compliance even in studies of rare conditions difficult to conduct in the U.S.

    IDR has an impressive record of 10 FDA inspections in the past nine years without any findings or observations.

    Contact Center or Provider

    Back to Listings

    Upcoming Events

    • 25Apr

      Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials

    • 26Apr

      FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know

    • 27Apr

      Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis

    • 17May

      2023 WCG Avoca Quality Consortium Summit

    • 21May

      WCG MAGI Clinical Research Conference – 2023 East

    Featured Products

    • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

      Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    • Surviving an FDA GCP Inspection

      Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

    Featured Stories

    • Five Ws

      Consider the Five ‘W’s to Understand Potential Participants

    • QandA-360x240.png

      Perspectives from Smaller-Sized CROs: Q&A with Cheryle Evans

    • White House

      Trial Stakeholders Advise White House on Emergency Research Infrastructure

    • SurveywBlueBackground-360x240.png

      Stress Levels Continue to Climb in Healthcare Workforce, Survey Finds

    Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

    The information you need to adapt your monitoring plan to changing times.

    Learn More Here
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 617.948.5100 – Toll free 866.219.3440

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing