CT&T is a privately owned Contract Research Organization (CRO) that provides clinical research services to the pharmaceutical and medical device companies. Our trained team members are the experts to call when you want your clinical study to succeed, whether you are a local or international company, a study investigator or a clinical research institute.

CT&T offers a full range of services to plan, support and manage the clinical research process professionally and accurately from Phase I through Phase IV, including investigator initiated trials.
All services comply with ICH-GCP guidelines, international and local applicable regulatory requirements.

In addition to comprehensive knowledge and experience in the clinical trials environment, CT&T offers vital strategic alliances with full service clinical research organizations saving our clients valuable time and reducing their overall costs.

The key to our success is our experience, expertise and dedication of our team.

Our goal is to provide our clients with high quality, tailor-made solutions that fit their budget and time constraints.

The proven effectiveness of our services commences at the start of the product development process and ends with the product's marketing.

Discover why investigators, pharmaceutical and biotech companies choose to work with CT&T.
CT&T has extensive experience in the design, implementation and conduct of clinical trials from Phase I through IV studies, feasibility and site selection, as well as non-interventional programs, follow-up studies such as post-marketing and drug surveillance studies. Our services provide all that is needed to meet study requirements such as:

  • Preparation of study protocol, IB, Informed consent, and other regulatory documents
  • Preparation of CRFs, worksheets, questionnaires, study-specific forms and patient tools
  • Ethics Committee & Competent Authority regulatory submissions
  • Project management and/or monitoring
  • Study coordination and site support
  • Training study staff and collaborating other cooperating units
  • Data management
  • Preparation of study and summary reports
  • Evaluation and selection of contract laboratory organization(s)
  • Clinical Quality Assurance audits
The Principle Investigator has the overall responsibility at the site, but can and should delegate roles and activities to other team members.

The Clinical Research Coordinator (CRC) is a crucial function at site for maximizing study management and performance. A well trained CRC will lead study related activities and make sure all requirements are met, thereby, releasing the investigator(s) to focus on the clinical aspects of the study and subject's mediacl care.

The advantages of employing a CRC through CT&T:

  • CT&T has a pool of academic manpower with various backgrounds for the optimal matching with the relevant protocol
  • Employing a CRC through CT&T avoids dealing with wages / conditions / complaints
  • CT&T can provide part-time / short periods employment according to your needs
  • CT&T can provide an immediate replacement if needed
  • CT&T structure is arranged to provide consistent availability and accessibility
  • CT&T provide professionalism
  • CT&T provide continuous training and support including a live help desk (technical issues / local procedures / international regulations) to their CRC for maximizing their knowledge in the field

The CT&T CRC will significantly release the investigator(s) from the administration burdens and study logistics while achieving accurate study management, efficient time management that results in costs saving as well as high quality performance of the site. The investigator’s time can then be dedicated to patient treatment and medical care. CT&T CRC are committed to your study performance on site.
CT&T is able to perform studies in any therapeutic area of medical care.

We have extensive experience based on our years of operation in various indications.

Our team members are well aware of the need to attain good and high quality source verified clinical data, within short time-lines, while complying with the study protocol, good clinical practice and regulatory requirements.

Our therapeutic areas of research include:
  • Anesthesiology
  • Cardiovascular and Cardiology
  • CNS (multiple sclerosis)
  • Dermatology
  • Diabetics
  • Endocrinology
  • Gastroenterology
  • Gynecology
  • Hematology
  • Infectious Disease
  • Neurology
  • Orthopedics
  • OSA
  • Pain management
  • Pulmonary Hypertension
  • Pulmonology
  • Wound Management
Among Our Clients:

  • FibroControl
  • Todos Medical
  • Collplant
  • VBL
  • Medtronic
  • Vasogen
  • Bayer
  • Gilead
  • MSD
  • Novartis
Office: 08-9398649
mobile: 052-5527548