The 10 recommendations of the 1st Biobanking Symposium on 12 & 13 November 2019
Start the biobanking project as a “pilot project” towards expansion to other structures
Implement a national information system centralised by the IRC.
Establish guidelines containing the criteria, standards and procedures (technical, organisational, regulatory and ethical) of a biobank belonging to the national network.
Train the new professions of “biobankers” and create a diploma for anatomopatology and genetics specialists. Continuous training for all those involved (surgeons, organ specialists, technicians ….)
Integrate any public structure respecting the guidelines into the national biobank network by being responsible for its own biobank.
Have standardised procedures for each type of cancer.
Harmonise the headings to be filled in for each patient/sample at national level in all centres in order to have a complete and uniform database.
Keep only tissues (healthy and tumour) and possibly serum in the first instance.
To have a single national scientific steering committee for the biobanking network, which will have among its missions to guide possible research projects. The Biobanks-OncO-Ma SPC will be responsible for:
– Initiate and coordinate Biobanking-Onco-Ma projects
– Ensure administrative and managerial follow-up
– Follow up the steps and deadlines associated with the different phases
– Edit a report to the different partners at the end of each phase
– Create scientific and technical expertise units and monitor their work at national and regional level.
Work as a network on all aspects.
