Clinical Data Management
- Capabilities
- Services
- Why us?
Clinical Data Management:
 
bullet Capabilities:
 
bullet CRF designing using standard tools such as Adobe® PageMaker® or Adobe® InDesign®
bullet Designing and implementing database using ClintrialTM 4.5
bullet Database designing within one week
bullet eCRF technology with SAS® PheedIt
bullet Data validation and clinical programming
bullet Data Management Plan and Data Validation Plan preparation
bullet Medical coding with proprietary coding dictionaries such as MedDRA®, WHODD
bullet Data review using “I-review” tool
bullet Sponsor access to clinical data through secured path using “J-Review” tool
bullet Solutions that adhere to consistent data standards such as CDISC and GCDMP
bullet QA process by dedicated QA team
bullet Ability to work on sponsors CDMS through Citrix

bullet Services:
 
bullet Data entry services
bullet Coding of adverse events and medications
bullet Lab data transfers per sponsor’s specifications
bullet Clinical programming
bullet Complete clinical data management services
 
bullet Why us?
 
bullet Ability to support operations round the clock
bullet Equipped with latest industry leading software tools like ClintrialTM 4.5, SAS 9.1.3, Oracle SAS® access, I-Review, J- review etc. deployed in a validated environment
bullet Latest versions of medical coding dictionaries of WHODD and MedDRA
bullet Certified clinical data managers
bullet Trained and certified in implementation of CDISC standards
bullet Strong team of experts who focus on innovative procedure to ensure 100% quality services
 

Lambda Therapeutic Research Ltd.
A CRO for Clinical Research, Clinical Trials, Medical Writing, Bioanalytical, Bioequivalence and Pharmacovigilance services.
India (Ahmedabad - Mumbai - Chennai), Poland (Warsaw), USA