Consulting
From strategic consulting to post-market follow-up, CEISO is always by your side, making sure every box is ticked as you work toward the commercialization of your products.
Quality-regulatory advice, audits, training, market access, post-market surveillance, clinical evaluation and investigation within our clinical department MediaClin: Continuity and complementarity drive our activity, with a focus on proximity, trust, and loyalty.
From strategic consulting to post-market follow-up, CEISO is always by your side, making sure every box is ticked as you work toward the commercialization of your products.
To ensure continuity between evaluation and investigation, CEISO manages all stages of your clinical trial (Design, Implementation, Coordination) within its clinical department, MediaClin.
A Qualiopi-certified company, CEISO offers customized training sessions, both in-person and virtual. Our e-learning platform provides access to regulatory and normative training on demand, tailored to your specific needs.
Are you looking to access the European and/or international market? Seeking a mandate holder or a PRRC? Are you aiming for your products to be reimbursed on the French market? CEISO is the support you need.
CE (European Conformity) + ISO (International Organization for Standardization) = CEISO!
Industrial companies, large international law firms, leading NGOs and humanitarian associations, as well as innovative startups: all structures and organizations of various sizes that have trusted and continue to trust CEISO to support them in the development of their projects.
Since its creation in 1999, CEISO has been able to attract and retain clients through the strength of its “one-stop-shop” offer, contributing to the efficiency of products throughout their lifecycle, from the design phase to the implementation of post-commercialization surveillance tools, including clinical evaluation. For the latter, CEISO has even integrated a clinical department, “Mediaclin”, dedicated to clinical trials (C.R.O.).
As a testament to its expertise, CEISO has obtained ISO 9001, ISO 13485, and Qualiopi certifications, as well as the CIR accreditation.
Through its comprehensive training program and personalized journeys, CEISO accompanies all economic operators in the Medical Device and In Vitro Diagnostic Medical Device fields in deciphering regulations. The goal being to enable all — from manufacturer to distributor, agent, importer, etc. — to understand the requirements and obligations they have to comply with, and bring their products and services to market.
Having received the Qualiopi certification in January 2021, CEISO is best positioned to ensure the personalized upskilling of your teams, whether it is through in-person or virtual classroom training, within your organization or beyond. All the while adapting to your professions and trades, for tailored support.
CEISO also offers an exclusive turnkey e-learning platform: “CEISO ACADEMY”, lighting the path to understanding and implementing the 2021 European regulations on Medical Devices (EU) 2017/745.
CEISO has invested in its organization by being evaluated by an international third party and obtaining ISO 9001, ISO 13485, and Qualiopi certifications, as well as the CIR accreditation. Learn more about our certifications.
ISO CERTIFICATIONS
Certified ISO 9001 and ISO 13485 (medical sector) by AFNOR Certification for all of our activities: Consulting, Clinic, Training, Mandate, and PCVRR.
TRAINING CERTIFICATION
CEISO is a QUALIOPI AFNOR Certified training organization.
CIR APPROVED
CIR Approval (Research Tax Credit), allowing our clients to benefit from tax relief in the development of their product.
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Consulting, Clinical Services, Training. We assist you in bringing your medical devices to market.