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

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

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.

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.

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.

Metrics

7.9 Hours

SAE Turnaround Time

3.05 Days

Feasibility Turn Around Time

28000

Patient Database

100%

QC Rate

4.46 Days

Contract Turn Around Time

0.7 Days

CDA Turn Around Time

4.2 Days

Enrollment Time (Green Light to FSFV)

113% Average

Enrollment vs. Promised

11.6 Days

Regulatory Submission Time

Clients

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

"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

"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

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