Leaders in the field in Phase I-IV patient-centric clinical trials.

Working with Vitalink provides me the opportunity to be up to date on cutting edge treatments and helps me understand the science behind the development of the newest medications that we have available for our patients.

— Luis Delacruz, MD

Principal Investigator, Greenville, SC

Leaders in the field in Phase I-IV patient-centric clinical trials.

Clinical research is important to because I feel that pharmaceuticals continue to help people live healthier and in some instances, longer lives. I enjoy the fact that it keeps me current with medicine that helps me take better care of my patients.

— David Godwin, MD

Principal Investigator, Greenville, SC

Leaders in the field in Phase I-IV patient-centric clinical trials.

Clinical research allows me to be on the cutting edge of my medical specialty as well as allowing my patients the unique opportunity to benefit from the latest innovation in their treatments.

— Bang Giep, MD

Principal Investigator, Spartanburg, SC

Vitalink Research, a US network of fully integrated clinical trial sites, connects world-class physicians and medical professionals with site managers and research coordinators to set the standard for the timely execution of clinical trial protocols with trustworthy results across all sites.

Therapeutic Areas:

  • COPD
  • Asthma
  • Internal Medicine
  • Phase I-IV/ Bioequivalence
  • Women's Health

The Vitalink Difference

Patient Centric Model

Patient Centric Model

We tailor medical care at all of our research sites to individual patients and place their safety and well-being above all else. Our facilities all have modern amenities and the comforts of home to ensure the best patient experience.

World Class PIs

World Class PIs

Our PIs are respected thought leaders dedicated to advancing the clinical research field. Each of our teams is ACRP certified to ensure every clinical trial operates at the highest level of efficiency with unmatched patient care, and accurate and timely data.

Dedicated Sites

Dedicated Sites

Vitalink Research sites are solely committed to clinical trials and patient safety to consistently achieve verifiable results. Our passionate teams work collaboratively using state-of-the-art equipment to bring their expertise and dedication across a variety of therapeutic areas.

Standardized Processes

Standardized Processes

Our innovative standard operating procedures and quality control and assurance processes are consistent across all sites so your information stays organized and accessible. We use one point-of-contact from feasibility to close-out so trials can be completed ahead of schedule, on budget, and with reliable results.

Metrics

11.6 Days

Regulatory Submission Time

28000

Patient Database

4.46 Days

Contract Turn Around Time

4.2 Days

Enrollment Time (Green Light to FSFV)

3.05 Days

Feasibility Turn Around Time

0.7 Days

CDA Turn Around Time

113% Average

Enrollment vs. Promised

7.9 Hours

SAE Turnaround Time

100%

QC Rate

Clients

IncResearch
Novartis
PRA
Pearl
Dey
ForestLaboratoriesInc
Mylan
Roche
PremierResearch
Genentech
Intentiv
BoehringerIngelheim
Quintiles
Ardea
Pearl
Synteract
Takeda
Theravance
Quorom
Chiltern
pfizer
Teva
astrazeneca
Covance
GSK
PPD
WCG
Parexel
Sunovion
Schulman

VitaLink delivered 130% faster and 380% more than the AVERAGE group in the US

-Parexel, Director of Site Alliances

“We decided to work exclusively with Vitalink sites and we enrolled 100 COPD patients in one day. That blew our minds!”

-VP of Clinical Development

"If Vitalink contacted me and said they wanted to do a study with us, given their track record in internal medicine, I would certainly try to work with them"

-Global Head of Clinical Research

"Their managers are great...they are medically trained and have a keen understanding for research. That's different than a lot of sites. "

-Clinical Trial Auditor