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Next trainings : September 2010 |
Is scientific interest for you a great source of motivation ?
You wish to benefit from a continuing training of rare quality ?
You want to discover another relation with your patients ?
You wish to widen your field of professional action with a new source of revenue in connection with new competences ? If yes, TAKE PART IN A VALIDATED TRAINING FOR CLINICAL INVESTIGATORS
according to the guidelines of the European Science Foundation covering :
- The Good Clinical Practices (GCP) & the legal aspects.
- The methodology of the clinical trials.
- The practical methods.
- The critical reading of scientific literature and study protocols.
- The relation doctor - patient within the framework of a clinical trial.
And integrate our dynamic and convivial network ! The theoretical courses are illustrated by exercices and works in sub-groups. They are given by experienced investigators, university lecturers and trainers specialised in human relations.
We will be happy to meet you during this training to be able to talk about and share our projets with you and hope that at your turn you will want to invest you in medical research.
Our next DUTCH training will take place on Saturday 11th September 2010 (One day : 1st part only)
Place : Somedi, Liersesteenweg n° 267 at 2220 Heist-op-den-Berg (max. 15 persons)
Detailed view of the subjects seen during this initial training / Registration form
Our next FRENCH training will take place on Saturday 25th September 2010 (One day : 1st part only)
Place : ResearchLink, Rue de la Station n° 78 at 1630 Linkebeek (max. 15 persons)
Detailed view of the subjects seen during this initial training / Registration form
Target public :
All doctors interested in clinical research on the human person, that they are general practitioners or specialists, academic or not.
It is also addressed to nurses wishing to take part in clinical research as study nurses.
Objective :
This training is intended to provide all knowledge essentials to a doctor to become a good clinical research investigator.
It is given over two full days and includes all the lawful, legal and ethical information as well as the responsibilities of the investigator during all the stages of a clinical study.
Contents :
- Methodology of clinical research : Description of the framework, the various steps, the different actors and their respective roles.
- The regulation framework : The Declaration of Helsinki, the Good Clinical Practices, the European Directives, the Belgian law.
- The ethical framework : the various steps of a clinical study in particular, with case analysis and practical exercices in small groups.
Please note that the application for accreditation in Section 6 "Ethics and Economics" has been asked to the INAMI. |
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ResearchLink is the first and only Belgian Clinical Trial Network (CTN) dedicated to the success of clinical trials with general practitioners (GP's) for the pharmaceutical industry.
Created by GP investigators, ResearchLink is staffed by a team of experienced professionals, ensuring compliance with ICH / GCP quality standards.
Our investigators must meet specific criteria such as patient population, administrative capabilities to properly conduct clinical trials, enthusiasm, ... before joining our network. Each of them has been trained in Clinical Research - including the GCP's - thus allowing time and money saving to identify and enroll patients, and initiate a site.
At ResearchLink we focus on rapid set-up of studies and patient recruitment through a network of 120 family doctors.
The support we provide to our investigators allows them to concentrate on recruitment and clinical decisions.
As a result, monitoring costs for sponsors or CRO's are reduced, trial supply and documentation are simplified and quality data may be generated with less queries.
If you would like to know more about ResearchLink, check out what the press says about us by clicking here .
To get in touch withe someone of our team, please call +32-2-383 04 55 or send an e-mail to
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