CL01 – Systematic Literature Review Methodology
REF. CL01 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a product’s compliance with the general requirements must
You work in a demanding regulatory and normative environment. The effectiveness of your collaborators is an essential element of your company’s performance. We support you in the development and maintenance of your team’s skills.
All our trainings can be conducted in INTER or INTRA, in-person or in virtual class. We can also design customized trainings to meet your needs.
*IP = In-person / Virt. = Virtual class
| Training | Ref. | Duration | Price (excl. taxes) INTER (€) | Jan. 23 | Feb. 23 | Mar. 23 | Apr. 23 | May 23 | Jun. 23 |
|---|---|---|---|---|---|---|---|---|---|
| Systematic Literature Review Methodology | CL01 | 1 day 7 hours | 800,00€ | ||||||
| Clinical Evaluation of a Medical Device | CL02 | 1 day 7 hours | 800,00€ | ||||||
| Clinical Evaluation and Literature Review Methodology | CL03 | 1,5 days 10,5 hours | 1200,00€ | ||||||
| Good Clinical Practices according to ISO 14155 | CL04 | 1 day 7 hours | 800,00€ | 13/01 - Virt. FULL | 08/06 - Virt. ou Prés. Orsay | ||||
| Clinical Investigations of Medical Devices | CL05 | 1 day 7 hours | 800,00€ | ||||||
| Clinical Investigations and Good Clinical Practices according to ISO 14155 | CL06 | 1,5 days 10,5 hours | 1200,00€ | ||||||
| Clinical Performance Study for an In Vitro Diagnostic Medical Device | CL07 | 1 day 7 hours | 800,00€ | 23/05 - Prés. FULL | |||||
| Clinical Performance Evaluation of an In Vitro Diagnostic Medical Device | CL08 | 1 day 7 hours | 800,00€ | ||||||
| Post-Market Clinical Follow-Up of a Medical Device | CL09 | 1 day 7 hours | 800,00€ | ||||||
| Post-Market Performance Follow-Up of an In Vitro Diagnostic Medical Device | CL10 | 1 day 7 hours | 800,00€ |
REF. CL01 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a product’s compliance with the general requirements must
REF. CL02 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a Medical Device’s compliance with the General Safety
REF. CL03 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of compliance with the General Safety and Performance Requirements
REF. CL04 – INTRA / INTER CLINICAL COURSE DESCRIPTION Clinical development and post-market clinical follow-up of a Medical Device may
REF. CL05 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a Medical Device’s compliance with the General Safety
REF. CL06 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a Medical Device’s compliance with the General Safety
REF. CL07 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of the product’s compliance with the general requirements of
REF. CL08 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of the compliance of an In Vitro Diagnostic Medical
REF. CL09 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of a Medical Device’s compliance with the General Safety
REF. CL10 – INTRA / INTER CLINICAL COURSE DESCRIPTION The demonstration of an In Vitro Diagnostic Medical Device’s compliance with
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Consulting, Clinical Services, Training. We assist you in bringing your medical devices to market.