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Statistical Programming
Expert execution for successful regulatory submissions
For the clinical research industry, high-quality statistical programming with consistency and scalability has always been a roadblock. Our statistical programming teams have a robust track record of delivering a wide range of outputs, with consistent quality, leading to successful regulatory submissions. Several submissions supported by Algorics have been approved with products on the market today. Be it a complex program, therapeutic area expertise or an urgent need to scale your internal statistical programming capabilities, our team is invested in your success every step of the way.
80
Biostatistics and programming staff
95
Studies delivered to date
20
DMCs handled
Experts
In Oncology, Vaccines, Medical devices
Successful
FDA and EMEA submissions
eCRF creation, CDISC package creation to eSubmissions
Tables, listings & figures (TLFs)
Safety monitoring, interim analysis & annual report
Analysis of BA/BE studies
Study analysis and reporting
Analysis of safety, efficacy data for CSR, and regulatory submissions
Exploratory analysis
Meta-analysis
SDTM/ADaM/analysis data sets
Patient profiles
ISS/ISE
DMC/DSMB services
Case Study
Learn more about how our team helped navigate a complex ISS/ISE submission
Brochure
Download to learn how our biometrics solutions can help you augment internal expertise and capacity in record time
Efficiencies augmented by MetaVate, our unique data transformation engine
Delivered complex regulatory submissions for FDA and EMA approvals
Track record of consistent high-quality output
98% repeat business