CSR – REACH Authorisation decisions – Triton X-100 – Ortho-clinical-Use1
CSR – REACH Authorisation decisions – Triton X-100 – Ortho-clinical-Use2
EU – Chemical Safety Report – CSR – REACH Authorisation decisions – Triton X-100 – Ortho-clinical-Use1
Published in Europe and Regulation on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
More from EuropeMore posts in Europe »
- EU – Guidance – Clinical evaluation assessment report template
- EU – Checklist for EN 17466 & Validation (Instructions for use for reusable & re-sterilisable medical devices)
- EU – Team NB position statement on the requirements for the EU MDR/IVDR Notified Body Partners under the Technical Cooperation Program on Exchange of Medical Device Quality Management System Regulation and ISO 13485 Audit Reports (TCP III)
- UK – MHRA – Medical Device “Certificates of Compliance” / “Attestation of Conformity” have no legal standing under MDR
- EU – Availability and capacity of notified bodies to carry out conformity assessments for COVID-19 related medical devices and in vitro diagnostic medical devices
More from Regulation on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)More posts in Regulation on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) »
Be First to Comment