Biostatistics & Programming
- Capabilities
- Services
- Why us?
Biostatistics & Programming:
 
bullet Capabilities:
 
bullet Supports clients through the entire process of drug discovery and development of medical devices, spanning all phases of clinical research
bullet Comprehensive support for bioavailability/bioequivalence studies, all phases of clinical trials in patients, as well as pre-clinical animal studies
bullet Support on fixed sample size trials, sequential studies and adaptive designs
bullet Department is furnished with SAS version 9.1.3 for randomization, statistical analysis, TLGs and sample size calculation and WinNonlin version 5.0.1 for PK/PD analysis
 
bullet Services:

bullet Inputs to Protocol
bullet Study design
bullet Sample size
bullet CRF review
bullet Randomization schedules
bullet Preparation of Statistical Analysis Plan (SAP)
bullet Statistical analysis
bullet Programming of tables, listings and Graphs (TLGs)
bullet Compliance with SDTM and ADaM standards if required
bullet Statistical reporting
bullet Preparation of SAS datasets as per CDISC principles
 
bullet Why us?

bullet Specialized in providing sophisticated statistical analysis planning and execution
bullet High quality data presentation and statistical report writing in accordance with global regulatory standards
bullet Team comprises of qualified/trained statisticians and SAS Programmers
bullet Clients trust Lambda to provide technical expertise, efficiency and flexibility with an emphasis on quality and timeliness


 

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