GHC Clinical Services https://validator.w3.org/feed/docs/rss2.html Home QMS SOPs SOP 20 – Conducting Site Audits SOP-38: Corrective and Preventive Action (CAPA) Management Documents SOP37 – Database lock and Unlock SOP36 – Data transfer SOP35 – Query Management SOP34 – Medical Coding SOP33 – SAE Reconciliation Plan SOP32 – Data Loading SOP28 – eCRF DESIGN & USER ACCEPTANCE TESTING SOP27 – CRF ANNOTATION SOP22 – Internal quality management at GCS SOP 19 – Sample Management SOP 18 – Drug Device Accountability Dispensation and Return SOP 17 – Recruting study subjects SOP31 – Data Entry Review and Validation (Paper CRFs) and Data Entry Review and Validation (eCRFs) SOP15 – Privacy and Confidentiality SOP9 – Preparation and management of study files (Trial Master File & Investigator Site File) and Clinical study forms and logs. SOP30 – CRF Completion Guidelines SOP3 – Confidentiality Disclosure Agreement (CDA) Quality Manual GCS SOP29 – EDIT CHECK PROGRAMMING QMS11 – GCS Change Control Procedure QMS10 – GCS Complaint Management QMS9 – GCS Risks Opportunities Register QMS8 – GCS Quality Policy QMS7 – GCS Organisation chart QMS6 – GCS Nonconforming Outputs Form QMS5 – GCS Internal Audit Procedure QMS4 – GCS Document Control Procedure QMS3 – GCS Company Objectives QMS2 – GCS New Starter and leave Form SOP1 – Preparing SOPs QMS1 – GCS CAR Form SOP 16 – Data Safety Monitoring Plan SOP14 – Reviewing the Informed Consent form and Obtaining Informed Consent SOP13 – Study Monitoring SOP12 – Communication practices between Site and Sponsor or CRO SOP11 – Site Study Team Responsibilities SOP10 – Interactions with EC SOP8 – Essential Documents Development SOP26 – Statistical Analysis Plan SOP21 – Study Team CRO Staff Training SOP25 – Data Management Plan SOP24 – Monitoring, Evaluation, And Reporting Of Safety Data SOP23 – Management of regulatory aspects related to clinical trial SOP7 – Lab Selection