Clinical Monitoring

 

     
Convex offers a full range of monitoring services in:

 

  • Phase I–IV studies on drugs
  • Bioequivalence and bioavailability studies
  • Clinical studies on food supplements
  • Clinical studies on medical devices
  • Clinical studies on vaccines

 

Convex monitoring team consists of full time Clinical Research

Associates who guarantee up-to-date knowledge of the clinical

trials’status at each clinical site. Our monitoring procedures include:

 

  • Evaluation of the study’s progress
  • Review of the staff and facilities at the clinical sites
  • Review of Protocol compliance
  • Review of CRFs and performance of SDV
  • Review of Investigator’s File
  • Review of Biological Sample Handling
  • Review of Investigational Product(s)
  • Implementation of Corrective Actions
  • Addressing Administrative Issues
  • Maintaining tracking reports, etc

 

Our well trained CRA team allows your project to stay in

progress.  We have been delivering accurate data for

our clients for over 240 successfully completed clinical projects.

 

Our CRA strenghts are:

 

 

  • Exceeds expectations in all areas
  • Knowledgeable and efficient
  • Responsive to phone calls or emails
  • Organized and has good teaching skills
  • Teamwork is exceptional
  • Communication is outstanding

 

We cover the following therapeutic areas:                            

 

  • Allergology
  • Respiratory tract diseases
  • Dermatology
  • Oncology
  • Cardiovascular Diseases
  • Ophtalmology
  • Pain Management
  • Central Nervous System
  • Endocrinology
  • Haematology
  • Gastroenterology
  • Musculoskeletal disorders
  • Vaccines
  • Food supplements
  • Paediatrics