Global Clinical Trials

Delivering excellence in clinical research through comprehensive trial management and successful patient outcomes

ALVEOGYL Medical Device Study

Successfully completed clinical trial for Post-Extraction Dry Socket treatment across India and France.

  • 14 locations in India
  • 2 locations in France
  • 90 patients enrolled
  • Comprehensive dossier preparation
  • Regulatory submissions & approvals
  • Timeline adherence

Oncology Study - Non-Hodgkin's Lymphoma

Top recruiting country for Phase III clinical trial of CD20 positive Indolent non-Hodgkin's Lymphoma treatment.

  • 40 patients enrolled
  • 12 clinical sites
  • Full service management
  • Regulatory approvals
  • Project monitoring
  • Drug depot management

Type II Diabetes with Chronic Renal Insufficiency

Successful rescue of struggling Phase III comparator study with enhanced recruitment strategy.

  • 45 patients enrolled
  • Exceeded target of 36
  • Multiple site management
  • Efficient recruitment
  • Timeline recovery

Diabetes Mellitus with Inadequate Glycemic Control

Comprehensive clinical trial for diabetes management with focus on glycemic control optimization.

  • Multi-center study design
  • Patient stratification protocols
  • HbA1c monitoring
  • Safety assessments
  • Efficacy evaluations

Diabetes Mellitus with Inadequate Glycemic Control on Insulin

Specialized study for insulin-dependent patients with suboptimal glycemic control.

  • Insulin optimization protocols
  • Continuous glucose monitoring
  • Patient education programs
  • Hypoglycemia risk assessment
  • Quality of life measures

Clinical Trial Expertise

Comprehensive capabilities across all aspects of clinical trial management.

Project Management

  • Expert protocol development
  • Comprehensive feasibilities for studies
  • Timeline optimization
  • Risk management
  • Quality control

Site Management

  • Site identification & selection
  • Investigator meetings
  • Staff training
  • Documentation management
  • Patient recruitment

Regulatory Compliance

  • DCGI submissions
  • Ethics committee approvals
  • Safety reporting
  • Regulatory inspections
  • SOP development