| Thumbnail | Title | Filename | Date Posted | Size |
|---|---|---|---|---|
 |
Trial Closure and End of Trial Reporting (SOP 021).pdf | SOP021_Trial_Closure_End_of_Trial_Reporting_Version_5.0_FINAL_26.04.23.pdf | 9/24/18 | 296.67 KB |
|
SOP023 Financial Procedures for Research Projects | SOP023_Financial_Procedures_for_Research_Studies_Version_6.0_FINAL.pdf | 9/24/18 | 1,003.40 KB |
|
Contract Negotiation and Review (SOP 024).pdf | SOP024_Contract_Negotiation_and_Review_Version_5.0_FINAL.pdf | 9/24/18 | 552.66 KB |
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SOP025 Assessment and Registration of Trust Risk Rating for Research Studies | SOP025_Assessment_and_Registration_of_Trust_Risk_Rating_for_Research_Studies_v8_FINAL.pdf | 9/24/18 | 844.41 KB |
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SOP029 Management of R&D Freezers | SOP029_Management_of_RD_Freezers_v5.pdf | 3/4/25 | 847.99 KB |
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SOP031 Patient Recruitment | SOP031_Patient_Recruitment_version_5.0.pdf | 10/20/22 | 212.54 KB |
 |
Trust Confirmation of Capacity and Capability & Sponsor Green Light to Conduct Research Studies (SOP034) | SOP034_Trust_Confirmation_of_C_and_C_to_Conduct_Research_Studies_V11.docx | 9/24/18 | 2,622.71 KB |
|
SOP035 Using the Local Portfolio Management System (EDGE) | SOP035_Using_the_Local_Portfolio_Management_System_v9.0.pdf | 9/24/18 | 1,377.63 KB |
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SOP037 Amendments to Research Studies | SOP037_Amendments_to_Research_Studies_Version_9.0_signed.pdf | 9/24/18 | 471.33 KB |
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SOP040 Management of External Research Staff - Research Passport Scheme | SOP040_Management_of_External_Research_Staff_Research_Passport_v7.0.pdf | 9/24/18 | 945.33 KB |
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SOP041 File Notes | SOP041_File_Notes_v_6.0.pdf | 9/24/18 | 766.61 KB |
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SOP048 Royal Papworth Sponsorship of Research Studies | SOP048_Applying_for_Papworth_Sponsorship_version_6.0.pdf | 9/24/18 | 829.18 KB |
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SOP049 GCP Training for Research Staff | SOP049_GCP_Training_for_Research_Staff_v6_FINAL.pdf | 9/24/18 | 655.70 KB |
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SOP 050 Protocol Non Compliance | SOP050_Handling_of_Non-Compliance_Version_7.0.pdf | 10/1/19 | 898.37 KB |
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Serious Breach of Protocol or GCP in CTIMPS and Non-CE Marked Devices (SOP 051).pdf | SOP051_Serious_Breach_of_Protocol_or_GCP_in_CTIMPs_and_Non-CE_Marked_Devices_v5.0_FINAL.pdf | 9/24/18 | 431.63 KB |
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SOP052 Dealing with Misconduct and Fraud Good Research Practice | SOP052_Misconduct_and_Fraud_Good_Research_Practice_v4_FINAL.pdf | 9/24/18 | 1,025.42 KB |
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SOP055 Roles and Responsibilities for the Conduct of Research Studies and Clinical Trials including CTIMPs | SOP055_Roles_and_Responsibilities_V4.0_FINAL.pdf | 9/24/18 | 856.39 KB |
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Version Control of Study Documentation (SOP 060).pdf | SOP060_Version_Control_of_Study_Documentation_Version_4.0_FINAL.pdf | 9/24/18 | 323.99 KB |
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Preparation of Regulatory Progress Reports including Periodic Safety Reporting and Annual Reports (SOP 062).pdf | SOP062_Preparation_of_Regulatory_Progress_Reports_version_6.0_FINAL.pdf | 9/24/18 | 392.92 KB |
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Research and Development Internal Good Clinical Practice (GCP) Audit (SOP 063).pdf | SOP063_GCP_Audit_v4.0_FINAL_signed.pdf | 9/24/18 | 341.20 KB |
Featured Events
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Date of event: Mar 4, 2026, 9:30 AM – 4:30 PM
The course is aimed at anyone seeking an introductory course on clinical trials and who is likely to be involved in the design, conduct, management and reporting of clinical trials.
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Date of event: Mar 11, 2026, 9:00 AM – 4:00 PM
The course is aimed at anyone seeking an introductory course on clinical trials and who is likely to be involved in the design, conduct, management and reporting of clinical trials.
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Date of event: Mar 18, 2026, 9:00 AM – 4:00 PM
The course is aimed at anyone seeking an introductory course on clinical trials and who is likely to be involved in the design, conduct, management and reporting of clinical trials.
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