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CEBIS is a Global Full Service Contract Research Organization (CRO) which provides clinical stage, regulatory and market entry support to biotech, pharmaceutical, medical devices and nutraceutical companies.
Phase II-IV
Interventional
Studies
Observational
Studies
Regulatory
Interventional Studies
(before the CE Mark)
Observational Studies
(after CE Mark)
New Claim Approval
Studies
Food Research &
Evaluation Studies
ISO 27001:2013 – Management Systems for Information Security appliable for all CEBIS divisions.
ISO 13485:2016 – QMS for Medical Devices.
ISO 22301:2020 – Security and resilience — Business continuity management systems appliable for all CEBIS divisions.
ISO 45001:2018 – Occupational health and safety management systems appliable for all CEBIS divisions.
ISO 9001:2015 – Quality management systems appliable for all CEBIS divisions.
ISO 14001:2015 – Environmental management systems appliable for all CEBIS divisions.
ISO 27017:2015 – Information technology — Security techniques — Code of practice for information security controls based on ISO/IEC 27002 for cloud services.
ISO 27018:2015 – Information technology — Security techniques — Code of practice for protection of personally identifiable information (PII) in public clouds acting as PII processors.
Following through on our commitment to address customers' needs we achieve excellence, being recognized by patients and other stakeholders as the company offering high quality services.
Even if you are still in the planning stages of your project, you are more than welcome to submit a request to us. We can assist you with a quotation or create a proposal for you based on the minimum information you can provide.
