Our services / Covering among others
  • Project Set-up & Delivery 
  • Risk Management
  • Third-Party Vendor Management 
  • Coordination of Various Fx Areas

  • Site Selection, Initiation, Monitoring and Close-Out Visits
  • Remote Monitoring Activities
  • Risk-Based Monitoring
  • Proactive Site\'s Personnel Support
  • Efficient Communications with Investigators
  • Analysis od Investigator Site Metrix
  • Motivational Visits on Site
  • Local Resources Managing Sites
  • Countries & Sites selection
  • Studies Feasibility Evaluation
  • Local Standard of Care Research
  • Study Execution Strategies
  • Sites Contracting
  • Sites Personel training
  • Sites Activation
  • Site-Specific Recruitment Plans & Execution
  • Study Sites Coordination
  • Study Advertisment & Awareness Programs
  • Recruitment Booster Startegies
RA Regulatory Affairs
  • Clinical Trial Applications for IMP and Device Studies     
  • Management of RA and IEC/IRB Review Process Amendments Classification and Submission
  • Legal Representation Services
  • Import/Export Requirements Expertise
SS Clinical Trial Supply Services
  • GMP, GDP Consulting and Assistance
  • Clinical Manufacturing Operations
  • Qualified Person Support 
  • Global Distribution and Storage
  • Clinical Development Planning
  • Clinical Trial Design
  • Scientific Advice (incl. EMA/FDA/NCA)
  • Regulatory Assistance
PV Pharmacovigilance
  • PhV Consulting and Assistance
  • Safety Management 
  • SAE Processing 
  • Expedited Reporting 
  • Periodic Reporting
MW Medical Writing
  • Clinical Writing (Protocol, IB, ICF, Study Report)
  • IMPD/CTD Development 
  • Scientific Publication Assistance
  • Medical Editing
MM Medical Monitoring
  • Medical Data Review
  • Scientific Support
  • Medical Trainings
  • Medical Opinion Leaders Expertise
P1 Phase 1 services in healthy volunteers
  • Early Product Development
  • First-in-Man Studies
  • Special Population Studies 
  • Proof of Concept Studies
  • PK/PD Studies 
  • eCRF Design and Data Validation Development
  • EDC Study Development  and User Acceptance Testing
  • Continuous Data Review and Query Management
  • Coding of Adverse Events, Medical History and Concomitant Medication
  • Database Lock and Archive
  • Trial Design Including Sample Size and Protocol Development
  • Data Validation Reports - Completeness and Correctness of Data
  • Preparation of CDISC Standard SDTM/ADaM Data Sets
  • Statistical Analysis (Interim and Final)
LD Learning & Development
  • ICH GCP Investigator Site Personnel Training (Attested by TransCelerate BioPharma Inc.) 
  • Induction & Continuous Training for Trial Execution Services 
  • Development Programs for CRAs and CTAs 
  • Therapeutic Area Trainings 
  • Tailored Educational Solutions for Sponsor 
QA Quality Assurance
  • Investigational Site Audit 
  • Co-Monitoring Visits 
  • Audits of Trial Master Files 
  • Process Audits
  • Subcontractor Audits: GCP, GLP, GMP Area
  • SOP Eriting and Review
LS Central Lab Services

  • Core Laboratory Testing Services
  • PK/PD analysis
  • Genomics
CI Central Imaging
  • ECG 
  • MRI
  • PET/CT
  • DEXA
  • Angiography
  • Provided directly by KCR
  • Provided by Preferred Providers
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We are an international full-service Contract Research Organization with a knowledge, experience and infrastructure that allow us to conduct any clinical trial, from a single site local study to multi-center programs spanning different regions. We provide comprehensive trial execution services for pharmaceutical, biotechnology, and medical device companies all around the world.

We translate sponsor’s goals into success.

Therapeutic Areas:

  • Cardiovascular
  • Dermatology
  • Endoctrinology
  • Gastrointestinal
  • Healthy subjects
  • Hematology
  • Immunology
  • Infectious Diseases
  • Nephrology
  • Neurology
  • Oncology
  • Ophtalmology
  • Orthopedics
  • Otorhinolaryngology
  • Psychiatry
  • Respiratory
  • Rheumatology
  • Surgery
  • Transplantology
  • Urology
  • Women's Health

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