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Clinical Data
Management:
Lambda
offers data management services in pre-clinical,
bio-equivalence and phase I-IV clinical
trials for both paper based EDC studies.
Though we are end-to-end service
providers,
we also offer services with maximum flexibility:
sponsors may contract all or a part of
their work to Lambda. We have a strong
team of experts who focus on innovative
procedure to ensure 100% quality services.
We are equipped with most sophisticated
tools like ClinTrial®, Pheedit, Oracle
SAS® access, I-Review, J- review, Winolin,
etc. deployed in validated environment.
Our Clinical Data Management services
include:
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CRF designing using standard tools such
as Adobe® PageMaker®
or Adobe InDesign® |
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Designing and implementing database using
ClinTrial® |
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eCRF
technology with SAS®
Pheedit |
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Capable
to have complete second entry
(Blind/Interactive) |
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Data
validation and clinical programming |
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Medical coding with proprietary coding
dictionaries such as MedDRA®, WHO
DD |
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Data review using integrated review tool |
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Sponsor
access to clinical data through secured
path using J-Review
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