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CONTINUING EDUCATION

The demand for high qualified clinical research professional is increasing significantly, as the organizations understand that talented and qualified personnel are key to superior competitive advantage. Providing quality ongoing training is also our commitment. The Intrials Continuing Education Program – ICEP focus on the planning, development and follow-up of all clinical trial processes. It is designed to meet the training needs of all professionals that are directly or indirectly involved with clinical research, and to promote the practice of Clinical Research Excellence (CRE).

The ICEP combines theory and practice related to clinical trials management in an continuously-changing scientific environment. The program method stimulates participant interaction and discussions of real-world issues using actual situations. The participants are stimulated to formulate strategies that are designed to ensure Clinical Research Excellence and Good Clinical Practice in all activities of the clinical trial processes.

INTRIALS WORKSHOP 2008
was a great success!
More...

ICEP Courses

1. Clinical Research Development
·	Objective: discuss the concepts, key processes and goals of clinical research; describe the basic concepts related to brainstorming as a tool to improve idea to creative problem-solving processes.

2. Good Clinical Practices (ICH-GCP)
·	Objective: describe and discuss the role and key concepts of GCPs to ensure Clinical Research Excellence.

3. Quality Assurance And Fraud Prevention In Clinical Trials
·	Objective: define the basic guidelines related to quality assurance in clinical trials and describe the most important measures the research community can take to prevent misconduct.

4. Improving Patient Recruitment Efficiency
·	Objective: provide an overview of key issues regarding patient recruitment in both not complex and highly complex studies, and discuss techniques to improve recruitment efficiency.

5. Biostatistics In Clinical Research For Non-Staticians
·	Objective: discuss the role of biostatistics in clinical research planning and design, as well as in reporting clinical trials results, use of statistics methods for sample size and data management.

6. Study Coordinator Practice
·	Objective: enhance technical skills and competence needed for a study coordinator professional. discuss basic and advanced concepts of site management and the role of the Clinical Research Associate in ensuring site compliance.

7. Pharmaco-Economics In Clinical Research
·	Objective: to learn the principles of economic assessment applied to pharmaceuticals, and demonstrate the cost-benefit relationship of a product, procedure or process.




INTRIALS WORKSHOP 2008 WAS A GREAT SUCCESS!! In order to share experiences with the clinical research society and contribute with knowledge expansion, INTRIALS has been promoting Workshop Sessions since 2002. In June 17th, 2008, INTRIALS staff presented the theory and the best practices in Clinical Research to 40 participants from pharmaceutical industries, biotechnology companies, hospitals and research centers in Brazil. Below are some of the testimonials. “Congratulations for the Workshop, ideas like this course is what we constantly need to improve our work quality and get updated” “In my opinion, the course was very good because it has put together all the “pieces”of clinical research themes, providing us with a systematic vision. The case studies presented help the professional knowledge as well” “Funny shaped serious information. It is impossible not to learn! INTRIALS WORKSHOP 2009 WILL BE ON JUNE 23, 2009FOR MORE INFORMATION AND ENROLMENTS, PLEASE MAIL TO vivian@intrials.com.br