change/insert date & location via >insert >header & footer 1. check in date & time...
TRANSCRIPT
![Page 1: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/1.jpg)
Clinical Study DataProcesses@ LEO Pharma
p. 01
April 21, 2023
![Page 2: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/2.jpg)
Process overviewApril 21, 2023
p. 02
eCRFOracle Clinical- MedDRA- WHO DrugCRO’s
CDISC- SDTM- ADaM- Controlled TerminologyOpenCDISC
TablesFiguresListingsAnalyses21 CFR part 11- Repository
eDocDefine.xmlPoolingPublishSubmission
![Page 3: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/3.jpg)
CDC repository
Data Capture and Management
• CRF pages built in OC◦Standardisation critical
• CRF pages from eCRF• Data Management in OC◦MedDRA◦Who Drug
• CRO outsourcing◦Standardisation critical
• SDTM◦From 2005◦Standardisation benefit & critical
• OpenCDISC Validator◦Standardisation benefit
April 21, 2023
p. 03
SDTM
OC
CRO
OpenCDISCValidator
eCRF
![Page 4: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/4.jpg)
CDC repository
Standards and Validation• Depends on standard
SDTM• ADaM since 2006• Standards allow for study
variations• Standards covers format,
not contents• Complex• 21 CFR part 11 compliant
April 21, 2023
p. 04
SDTM ADaM
Metadata
SAPU
SAS Code
![Page 5: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/5.jpg)
CDC repository
TFL and Statistics• Standardised/modifiable• Parameter based• Partly automated• Configurable• Analyses not standardised• Analyses ad-hoc per study• 21 CFR part 11 compliant
April 21, 2023
p. 05
SDTM
ADaM
TFL
Metadata
Spread sheet
SAS Code
![Page 6: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/6.jpg)
CDC repository
Reporting and Submission
• Not always performed• Pooling dependent of standards• define.xml ditto (documentation)• If data standardised,
submissions in weeks• Closed transfer between
validated systems• 21 CFR part 11 compliant
April 21, 2023
p. 06
Study data
Pooleddata
define.xml
eDoc etc.
eDoc Publish
![Page 7: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/7.jpg)
QC processes
• Risk based QC strategy• The most important and most critical parts• Primary and secondary end points• QC of additional parameters if applicable• Applies to CRF, SDTM, ADaM, Tables, Listings,
Figures, Analyses, Poolings, define.xml and everything else relevant
• Any deviation from standards requires additional QC• Greater adherence to standards yields shorter
production time of input to the CSR (months => weeks)
April 21, 2023
p. 07
![Page 8: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/8.jpg)
Conclusions• Clinical Study Data Processes are quite mature• Years of experience in CDSIC standards• 21 CFR part 11 compliant end-to-end• Strong focus on standards yields◦Automatisation◦Flexibility◦Quick CSR
• More elements needs to be standardised◦Protocol, CRF, Figures, Analyses, define.xml, Pooling,
Submissions, Data standards upgrades
April 21, 2023
p. 08
![Page 9: Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply](https://reader036.vdocument.in/reader036/viewer/2022062803/56649cd65503460f9499e0c4/html5/thumbnails/9.jpg)
QuestionsApril 21, 2023
p. 09