The capabilities of our research institute

More than 20 years of experience in a broad range of clinical trials related to dermatology, both medical and aesthetic dermatology, across all therapeutic interventions (drugs, biologics, devices) and dosage forms (topical, oral, injectable, IV).

We have worked on the full spectrum of dermatology trials - Studies ranging from Phase 1 to Phase IV safety and efficacy trials, from large multi-center studies to investigator-initiated trials, and all types of studies in-between.

Led by leading clinical research dermatologist, Dr. Stacy R. Smith, who has conducted clinical trials that have led to the FDA approval of numerous advancements and innovations in dermatology.

Our experienced research team is highly qualified and committed to responsible research.

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Indications evaluated at CDCRI


Below are listed just a few of the many diseases for which we can perform trials:

  • Psoriasis
  • Atopic dermatitis
  • Acne
  • Rosacea
  • Onychomycosis
  • Actinic keratoses
  • Verruca vulgaris
  • Vitiligo
  • Wound healing
  • Male pattern baldness
  • Female pattern baldness
  • Alopecia areata
  • Varicose veins and telangiectasias
  • Hyperhidrosis
  • Photoaging and wrinkling
  • Scarring
  • Localized adiposity (abdomen & neck)

We are equipped for clinical research


Below is a list of our capabilities and assets:

  • Controlled storage with 24/7 temperature monitoring - room temp, 2-8 C, -20C and -80
  • ACRP certified Clinical Investigator
  • Certified Clinical Research Coordinators
  • Dedicated data entry personnel
  • Dedicated recruitment personnel
  • On-site sub-investigator for studies requiring an unblinded investigator
  • Electronic Diaries
  • Experience with most of the assessment tools used in dermatology: PASI, IGA, GAIS, EASI, SCORAD, CSSRS, SALT and many more
  • Dedicated monitoring space with copier/printer
  • On site venipuncture and specimen prep
  • IATA dangerous goods certification
  • Protocol review and consulting
  • Single Center Studies
  • Actigraphy
  • Proof of concept studies
  • Phase IV or Investigator-Initiated Studies
  • Serum or Plasma Pharmacokinetics
  • Tissue Pharmacokinetics
  • Prolonged Observation (12 Hours)
  • Lesional and Non-Lesional Biopsies
  • Electrocardiograms
  • Pulmonary function testing
  • Gravimetric Measurement
  • Specialized Photography
  • Lesion mapping and tattooing
  • Imaging Studies
  • Ultrasound assessments
  • Stepped Cohort Enrollment
  • Home visits
  • Clinical Conductor site Management software

We provide feedback to our sponsors

  • We understand what a sponsor wants to see at the end of a study (and what they DON’T want to see).
  • We keep an eye out for problems DURING the trial and will let you know if we see something.
  • We will let you know early on so adjustments can be made rather than waiting until the end and finding out there was a problem that now cannot be fixed.


We use only the best study subjects

  • We take the time to imagine how a subject may perform in a study and consider whether they are a GOOD subject for this study.
  • We work hard to provide a patient-centric environment that leads to reliable, satisfied subjects and maximizes study retention.


We understand the dermatology clinical research process

  • Dr. Stacy R. Smith has served as a consultant to many drug and device manufacturers.
  • His work has included development of scales to assess new endpoints, overall development programs as well as interaction with FDA before and during the process of FDA clearance or approval. Thus, Dr. Smith and his staff understand the development and approval process.
  • To some sites, the regulations and requirements seem onerous; at CDCRI we know that they are a necessary part of an overall scheme.

CDCRI’s Research Staff


We pride ourselves on having dedicated, well-trained persons doing their best to execute your trial to exacting standards. Typically a study will be covered by several staff members to ensure adequate coverage and manpower to see a trial through to completion. You will find our research staff have broad knowledge in:

  • …product development for dermatological research: Our staff understands where the sponsor is in their development timeline and are better able to understand the goals of any particular study.
  • …good clinical research practices in San Diego: Not just memorization of regulations but why things are done the way they are in clinical research.
  • …skin disease or dermatological condition under study: Our staff understands the unique requirements of patients with the condition, concomitant medications that are commonly seen, why washout durations have specific lengths and much more.
  • …the protocol and the unique requirements it may have: In research the protocol is often called “The Bible”, it helps to know it chapter and verse.

Monitor Resources

Our private monitoring room is available to all study monitors. We have designed this space with monitors in mind and have included the following:

  • Printer
  • Chart Cart
  • Shelving
  • Phone charger
  • Personal heater
  • Sticky notes

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