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GO(S)6 Part I (Rev 2/11)NATIONAL HEALTH SERVICE APPLICATION FOR INCLUSION IN THE FIRST PART OF THE OPHTHALMIC LIST All the terms of service which presently apply to opticians (optometrists and ophthalmic
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Clinical safety of a refers to the assessment and monitoring of the safety of a clinical trial or medical product.
The sponsor or authorized representative of a clinical trial is required to file the clinical safety report.
Clinical safety reports are typically filled out electronically through a designated regulatory platform.
The purpose of clinical safety reports is to ensure the ongoing safety and well-being of clinical trial participants.
Information such as adverse events, serious adverse events, and any safety concerns must be reported on clinical safety reports.
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