Medical Investigators

Our Investigators network is composed of a variety of specialties and certified in Good Clinical Practices. These Investigators have experience in several studies, providing them the knowledge that can only be earned by practice. Another added value is that they have a patient data base which helps accelerate recruitment.

Investigators

Study Coordinators

Our portfolio of Study Coordinators has personnel with the corresponding accreditations, the experience supporting different types of studies and the execution according to Good Clinical Practices.

Coordinators

Clinical Diagnosis and Research Laboratory

Clinical Diagnosis and Research Laboratory with renowned experience complying with Good Laboratory Practices, under ICH guidelines. The Laboratory´s ultimate objective is to execute their work with excellence, precision and in time.

Research Laboratory

Specialized equipment and personnel

Trial offers all the adequate infrastructure for clinical research, clinical monitoring, study coordination, drug storage and handling of regulatory affairs process.

and personnel

(CRO/SMO) Investigational Sites

With over 12 years in the market, we offer ethical and professional support in development, handling and management of clinical studies.

Investigational Sites
  • Hospital

    Hospital

  • Diagnostic Center

    Diagnostic Center

  • Clinical Laboratory

    Clinical Laboratory

  • Rehabilitation Center

    Rehabilitation Center

We are strategically located to service providers necessary.

Trial,S.A. strategically located to provide efficient service.

Located next to Multimedica Hospital, Diagnostic Center "Tecniscan" Clinical Laboratory "Carelab" and Rehabilitation Center "Nufit".

Services

Our range of specialized and innovative services... Contact Us

Investigators

We have a data base of Investigators by specialty, which have been certified in Good Clinical Practices and have experience handling clinical studies. This previous experience provides them the knowledge that is only acquired through practice.

Study Coordinators

Our Study Coordinators pool has personnel with the corresponding accreditations, as well as the necessary experience supporting different types of research projects and executing in compliance with Good Clinical Practice.

Study Drug Logistics

We are facilitators in the process of import, distribution to investigational sites and destruction of study drug, under the standards required by local legislation.

Study Drug Storage

We guarantee the storage and inventory control of study drug in depots that comply with quality, physical conditions (temperature and humidity), security, reliability and accountability requirements.


Local Laboratory

We have a Clinical Diagnosis and Research Laboratory with renowned experience complying with Good Laboratory Practices, under ICH guidelines. The Laboratory´s ultimate objective is to execute their work with excellence, precision and in time.

Clinical Monitoring

We facilitate the hiring of Clinical Monitors qualified to oversee data collection and investigational site execution, ensuring regulatory compliance. Our Clinical Monitors have previous audit experience.

Regulatory Affairs

Qualified personnel that manage the regulatory process (submission and follow-up until final approval) and the files for regulatory documents (Trial Master File).

Advisory Committee

Running a feasibility evaluation properly designed, allows the correct strategy in selecting the most suitable sites for the execution of a research project.


Feasibility and Selection

Feasibility Studies are an essential factor for a clinical project in the country.

Running a properly designed feasibility study, provides a proper evaluation and allows specific strategies to choose centers that are suitable for conducting a trial. In Trial, S. A. we evaluate:

  • Site Capabilities
  • Investigation Infraestructures
  • Personnel and Equipment

  • Regulatory requirements and deadlines
  • Local Institutional Review Boards / Independent
  • Ethical review committees Speeds

  • Patient population available
  • Probability that patients accept
  • Participate in the clinical testing


Therapeutic Areas

In Trial, S. A. we handle the following areas:

Trial, S. A.

  • Allergy / Immunology
  • Cardiovascular
  • Critical Care
  • Dermatology
  • Endocrine / Metabolism
  • Infectious Diseases

  • Gastroenterology
  • Genitourinary
  • Hematology
  • Immunology
  • Respiratory
  • Neurology

  • Obstetrics / Gynecology
  • Dentistry
  • Ophthalmology
  • Oncology
  • Ear, nose and throat (ENT)
  • Pediatrics

  • Radiology
  • Respiratory
  • Rheumatology
  • Respiratory Therapy
  • Urology


Contact Us

For details of our services... Contact us!

Contact Details

Trial, S. A.

Therapeutic Research Institute and Lab.

2da. Calle 25-19 zona 15 Vista Hermosa I Edificio Multimédica Oficina 902 Ciudad de Guatemala

Guatemala

(+502) 2385-7612 al

(+502) 2385-7615

services@trialresearch.org

Quick Contact

Contactarnos Trial, S. A.