NEW PHASE CLINICAL TRIALS services

PATIENT POPULATION

In addition to Geriatric, NewPhase Clinical Trials has the following Patient  Population available for studies:

Hispanic  55%
African American  25%
Caucasian  20%

NewPhase Clinical Trials provides the project management resources and technical expertise you need to be successful. A dedicated project manager is assigned to each study and is responsible for tracking and monitoring the entire trial process as well as acting as a direct liaison for clients.

Our proactive project management style identifies potential hurdles early on, where they are the easiest and most cost effective to resolve.


We are able to meet and exceed stringent timelines and budget requirements regardless of the size and scope of your project. Our goal is to assist you in getting your product to the market as quickly as possible.


We make it as easy and convenient as possible for subjects to participate in your trial and successfully meet all study protocols. We have the experience and skills to offer services to meet your specific trial protocols. We customize our services to meet your needs. If a trial protocol requires a blood draw every 24 hours for 20 days, or urine collection every second day for three weeks, we can do that.

We help keep trials on-schedule and on-budget while helping participants comply with complex and sometimes taxing trial requirements. Our specimen services can be customized to include blood, urine, ekg’s and many others, and our exam services include, health history, height and weight and much more.

We can tailor our staff to match whatever protocols you require. Whether you need phlebotomists to simply perform blood draws, nursing staff for more involved procedures we can provide the staff to match your study’s exact parameters.

SERVICES PROVIDED BY NEWPHASE CLINICAL TRIALS 

  • Study coordinator and support staff    
  • Complete study management    
  • Standard Operating Procedures (SOP’s)    
  •  Site Email address    
  • Clinic facility with all required equipment   
  • Centralized CDA & feasibility submissions and management    
  • Comprehensive follow-up with Sponsors/CRO’s
  • Centralized budget negotiations and management
  • Centralized regulatory submissions and management
  • Complete patient recruitment and management

For Information:

(305) 858-4300

​Research Studies