Veritas |

Project Management

The basis of a successful clinical study is well-planned and effective project management. VeritasCRO provides the needed organization, time management, and risk analysis; which are essential for a successful outcome in project management. The steps of a project are always prepared in with detail. By determining the high-level expectations such as the reasoning for the need of the project, its possibility of applicability, and requirements for completing the project; the preliminary stage of the project is designed. Integrity and continuity are the main components of an effective project plan. Duration, cost and performance of the project are compared in each step. Adjustments are done accordingly, which are significant for the process to be conducted correctly.

Details

Clinical Trial Protocol Writing

All clinical trials begin with a planning protocol and a detailed presentation of the trial’s all aspects. Clinical research protocols are of central importance in conducting clinical research. VeritasCRO has an organization which establishes procedures in basic subjects including feasibility and site selection, project design and protocol development. VeritasCRO has formed a project team dedicated to forming project designs in a logical manner, performing risk analysis and coming up with sustainable suggestions based on concrete evidence. The company executes and controls the whole process. The clinical trial protocol is an appropriate tool to highlight, accept and address ethical challenges specific to each study. Writing a detailed and complete protocol is an important step before starting a project. The protocol should be written simply and accurately, with all aspects clarified.

Details

Good Clinical Practice School

Good Clinical Practice (GCP) is a scientific and ethical quality standard for the initiation, conduction, monitoring and control, analysis, and reporting of a clinical research project. The goal of this standard is to preserve the rights, security and wellness of the volunteer as explained on the Declaration of Helsinki. The data collected which is in accordance with GCP, is made to be valid, complete, and well documented. These directions ought to be followed, when creating clinical research data to be presented to official institutions. We strongly believe that GCP training will acquire the staff with the essential and basic qualifications required for conducting clinical research. We suggest that the leaders or staff members of a particular study at least complete the GCP introduction course online or face to face.

Details

Data Management and Statistic

VeritasCRO can supply statistical guidance ranging from your project’s design to statistical analysis plan and CRF design. The Organization provides services of a variety, including data inputting during your project, query management, and writing of integrated or statistical reports. The basic reasoning behind the standard is that a tool is required to be created to overcome and amend/improve the situation. The clinical trial –including appropriate IT and data management systems- is of high quality, reliable and in accordance with GCP compatible resources. It is accepted that the design, implementation, coordination and analysis of clinical studies require a multidisciplinary expert approach. The main research team are basic researchers, sub-researchers, clinical monitors, data management team, clinical research coordinators.

Details

Manuscript Writing

A medical article is a printed report elaborating on the research results and provides the basis for communication on scientific issues. A medical writing is the basis for explaining and sharing research results. Our expert team of experienced medical doctors provides medical article writing services in the field of health sciences. VeritasCRO controls the flow of thought and consistency at every stage of the article, since originality is of high significance in the medical article. The writing of medical articles should focus more on the creative and intellectual aspects of research than on technical issues. Writing an article requires continuous improvement of knowledge and competencies in accordance with better and up-to-date scientific literature evidence.

Details

Quality & Metric Reporting

As a clinical research organization, Veritas CRO adheres to specific procedures for the monitoring and analysis of quality in determining how the service requested by the sponsor is met. VeritasCRO acts in accordance with the Quality Management System (QMS), which is based on the Good Clinical Practice Manual. Each staff member of VeritasCRO controls his/her own tasks as well as the ones performed jointly with other units. The company provides the training needed for the execution of this responsibility. Articles indicating ethical approval, consent of the participants, and source of funding have been associated with greater adherence to reporting guidelines.

Details

Clinical Trial Translations

Nowadays, clinical trials are governed by strict guidelines, a declaration outlining standardized ethical practices, mountains of paperwork, a heavy review process, and the ability to affect a multibillion dollar pharmaceutical industry. Every new drug must go through a clinical trial, Patient Reported Outcomes (PROs) must be evaluated, and the drug deemed safe for humans to consume and doctors to prescribe. The failure to do so within the ethical and specified guidelines could result in serious health risks, including patient fatality. Since clinical trials provide information on how to treat various ailments, each of these treatments will need to be tested and approved in each country. Thus, designing and implementing a well-designed clinical trial is critical.

Details