Controlled Document - do not download/save/print/photocopy
Cancer Clinical Trials Centre Standard Operating Procedure SOP No.: 17
Title: Archiving
Current Version No.: 3.3 Reviewed & Endorsed by STH Research: 07/03/2016 Approved: 15/03/2016
Effective Date: 24/11/2017
SOP Version History
Reviewed No Changes
Approved
Effective Date
1.0
12/12/2005
01/02/2006
31/01/2008
2.0
24/12/2007
01/02/2008
13/01/2011
3.0
21/05/2010
14/01/2011
14/10/2012
3.1
19/09/2012
15/10/2012
28/02/2015
3.2
13/01/2015
01/03/2015
17/04/2016
3.3
15/03/2016
24/11/2017
Version
Ended
CCTC SOP Front Cover v4.0 06/10/2017
SOP – Archiving Background Archiving in the context of clinical research relates to the collection of essential documents. Archiving material must be available for inspection by the Regulatory Authorities. This SOP can only relate to material stored in the Cancer Clinical Trials Centre (CCTC), the WPH Pharmacy Department and at the CCTC off-site archiving facility. Trial materials in other WPH departments and other hospitals involved in conducting the research must be subject to their own SOP. Procedure Who The Principal Investigator is responsible for the archiving of their research. Where appropriate, this may be delegated to the assigned Research Nurse, Data Manager or archive co-ordinators. The process of archiving is the responsibility of the CCTC Lead Data Manager or a delegated member of the DM team. Some commercial sponsors will arrange and pay for the archiving of site documents at an independent GCP compliant facility. The Sponsor should name individuals within its organisation who are responsible for archiving. The Sponsor however may devolve responsibility onto this local site. Access to archives shall be restricted to the named individuals responsible for the archiving. Only the Sponsor, Principal Investigator (or delegated representative) and relevant authorities should have access to archived data. When Archiving of all trial material should take place when the following apply: • The study has been closed by the Sponsor/Principal Investigator • All data queries have been resolved • The Sponsor/Principal Investigator has agreed to have the documents archived. On an annual basis (or sooner if required) the archive coordinators will arrange for archive material from the CCTC to be transferred to the off-site facility. Any pharmacy files that can be archived are transferred from Pharmacy and put together with the ISF to be transferred to the off-site archive. SOP 17 Archiving – v3.3 Finalised: 19.01.2016 Page 1 of 8
All archiving material should be archived for at least 15 years, unless otherwise specified by the sponsor. Every year, the CCTC central database will be checked for any material that has been archived for more than 15 years. This material could be retrieved and destroyed. However, before destroying any archived material, the Investigator should contact the Sponsor for approval. How Archived material may be archived in microfiche format provided that the data is legible and retrievable. Computer data may be stored in electronic form. Archived material will be stored in a location where they are easily retrievable and secure from flooding, fire, theft, vandalism and loss. Archived material can be stored either in the CCTC archiving room or CCTC off-site archiving facility. In the case of commercial clinical trials some of the essential documents will be archived by the sponsoring company who will then take responsibility for their safe storage. At the start-up meeting, responsibility for archiving should be discussed and where possible, be passed to the sponsoring company. Any patient notes should be clearly labelled on the front cover stating that the patient has participated in a research trial. This label will prevent these notes from being destroyed or microfiched until the date specified on the label. The archive coordinators will contact the Pharmacy Department to retrieve any files to be included in the annual archive process. All trial material should have any plastic covers removed to avoid data degradation from the condensation caused by such covers. Blank CRFs and duplicate copies of protocols, blank PIS, blank consent (same version and date) should not be archived – they should be destroyed in confidential waste or returned to the sponsor. Commercial studies must be stored in separate archive boxes to the non-commercial studies. All archived material will be logged on the CCTC central database. This database will hold the CCTC trial reference number, the location (cupboard number or offsite archive box number), the date archived and contents. SOP 17 Archiving – v3.3 Finalised: 19.01.2016 Page 2 of 8
If a request is made to access archived material, an entry must be made in the Archive Retrieval Log (Appendix 2) to ensure accurate recording of this process. The checklist in Appendix 1 indicates the documents that require archiving. Details of the off-site archiving facility can be found in Appendix 3. References STH Research Department SOP A127 - Archiving of Essential Documents Generated During Clinical Research, v1.3 01 August 2014
Standard Operating Procedure Cancer Clinical Trials ...
Mar 7, 2016 - appropriate, this may be delegated to the assigned Research Nurse, Data Manager or ... relevant authorities should have access to archived data. ... Archived material can be stored either in the CCTC archiving room or CCTC off-site archiving facility. In the case of commercial clinical trials some of the ...
Mar 7, 2016 - 1.0 Hazard Description. 1.1 Dry Ice is the solid form of carbon Dioxide (CO2). Dry ice is available for use in the form of pellets, slices or blocks and may be supplied loose or in insulated containers. 1.2 Dry Ice is very cold (-78.5°
track and give prior approval to control overrides or deviations from policies and procedures.' The aim of ... Corporate governance/06.2 Integrated Management System/6. Internal controls/Exceptions) ... It constitutes a deviation from established pro
Standard operating procedure. Title: Paediatric investigation plan from re-start of procedure (after clock-stop) to PDCO opinion. Status: PUBLIC. Document no.: SOP/H/3453 ... Committee Support Department in Procedure Management and Committees Support
Standard operating procedure â PUBLIC. SOP/V/4112 15-DEC-20. Page 6/10. 5.0. Final SA. 5.1. Adoption of scientific advice. 5.2. Send to applicant. No. 5.5. Clarification? 2.0. Yes. Yes. 5.3. Archive and update tracking. 5.4. Include in post- meetin
Nov 10, 2015 - Respiratory secretions, pus, fluid and wound swab culture. ⢠Plate the neat sample (â¥10µl) or wound swab onto one half each of blood agar,. MacConkey agar and Ashdown's agar then inoculate the sample or swab into selective broth.
2012 and after. 7. Definitions. EPITT: European Pharmacovigilance Issues Tracking Tool is a web- based system that tracks and monitors the safety of medicinal.
Department of Marketing Authorisations. Nooruse 1 ... or by e-mail. Ministry of Health. Office 4 â ... Direção Geral de Alimentação e Veterinária. Sistema Nacional ...
It is the responsibility of the Head of Paediatric Medicines Office to ensure that this procedure is adhered to. The responsibility for the execution of a particular part of this procedure is identified in the right-hand column of part 9. Procedure.
SOP/EMA/0101. Standard operating procedure for conducting checks for conflicts of interest when ... Managing Meeting Documents system. Paed Asst ... Establish timelines. Inform PDCO sec. and applicant. 4. Schedule adoption of Revision by. PDCO plenar
OnLine Database [2]. Microbial genome annotation consists of three stages: sequence data pre-processing, feature prediction, and functional annotation. Feature prediction .... gene prediction program [10]. Overlaps between predicted features of diffe
The Internal Audit Charter of the European Medicines Agency approved by the Management. Board;. ⢠European Medicines Agency Audit Manual;. ⢠to outline the procedure for establishing the auditors' risk assessment and assurance map;. ⢠to outlin
Signature: on file .... Document Records and Electronic Archive Management system. D-SD- .... Set up a meeting between the CHMP AD, PRAC AD, CAT AD if.
Procurement Support and Compliance (PCS) therein. 2. ... Financial Regulation applicable to the budget of the European Medicines Agency .... Bank details.
Introduction of two deadlines for submission of maintenance report: at time of submission of CHMP application (for accelerated review and type II variation) or at ...
The purpose of this SOP is to establish a single cross-agency procedure for the correct application of. Article 62 of the ... SOP updated to reflect new organisational structure and new/revised corporate control documents. 5. ... Sound financial mana
There was a problem previewing this document. Retrying... Download. Connect more apps... Mercury spill ... dure 2012.pdf. Mercury spill ... dure 2012.pdf. Open.
Apr 10, 2017 - supplementary information is submitted by relevant Marketing Authorisation ... Email template - PAM Submission â Timetable (TT) of signal ...
In addition to enrollment, cost, time and sometimes even data quality advantages, countries like Poland, China, India and Brazil are rapidly expanding markets that require local .... countries, challenging local conditions, and a big question: Which
foreign data. On the other hand, some countries don't want to contribute more than. 20-30% of a multinational trial's study subjects. In your pre-IND meetings, ask ... only patient-facing documents like informed consent forms need translation. ... pa
... the apps below to open or edit this item. pdf-1273\clinical-statistics-introducing-clinical-trials-s ... l-data-analysis-jones-and-bartlett-series-in-mathemati.pdf.
