About Us
ABOUT US
Incred CR is an organization formed in 2009 as a SDMO (Site Management & Development Organization) by a group of experienced Clinical and Healthcare professionals.
Services
SERVICES
Site Management is the most important component of the entire human research. As a Site Development & Management Organization (SDMO) our aim is to provide you clinical trial sites.
Expertise
EXPERTISE
Incred CR has Capabilities to cover almost all indication strating from Oncology to Allergic Diseases. If you are looking for a specialist, please contact us.
Business Model
BUSINESS MODEL
Exclusive Site Model is our most preferred business models for native site, where Incred CR will take care of entire clinical operations to manage the clinical trial operations.

 

 

 

 

 

Our Services
Incred CR
  • GCP Training Programmes
  • Clinical Trial Site Management
  • Consultation for Research Native Sites
  • Staffing for Clinical Trial Sites
  • Site Infrastructure, Facility & Spacing Plan
  • Clinical Trial Foundation Programmes
Services
GCP Training Programmes

GCP training is a separate training and is not basic human subjects protection training. GCP principles are specific to clinical trials and include international ethical and scientific quality standards for designing, conducting, recording, and reporting clinical trials.

Services
Clinical Trial Site Management

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Services
Consultation for Research Native Sites

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Services
Staffing for Clinical Trial Sites

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Services
Site Infrastructure, Facility & Spacing Plan

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Services
Clinical Trial Foundation Programmes

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Looking for specialist / specific needs in
Clinical Research?
Speciaity / Therapeutic Areas
  • Cardiovascular Diseases
  • Dentistry
  • Dermatology
  • Endocrinology
  • Gastroenterology
  • Hematology
  • Internal Medicine
  • Nephrology
  • Neurology
  • Neurological Surgery
  • Obstetrics & Gynecology
  • Opthalmology
  • Orthopedics
  • Oncology
  • Otolaryngology
  • Pediatrics
  • Psychiatry
  • Pulmonary Disease
  • Rheumatology
  • Urology & General Surgery
Incred CR Highlights
  • Ability to provide GCP trained clinical research.
  • Sites equipped with standard operating procedures.
  • Huge database of highly skilled, experienced and enthusiastic investigators having access to large patient population.
  • Dedicated and experienced Clinical Research Coordinators.
  • Nationwide coverage.
  • Efficient and centralized contract and budget resolution.
  • Strong working relationships with local and central IRBs.
  • Stable, effective and mutually beneficial working relationships with Investigative sites.
Our advantage
Clinical trials require strict adherence to protocol, extensive documentation, complete accuracy, compliance to ICH-GCP and other regulatory norms, an ethically sound patient recruitment strategy, and efficient site management.