Statistical Programming

Expert execution for successful regulatory submissions

Driving consistent results and long-term partnerships

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.



Biostatistics and programming staff



Studies delivered to date



DMCs handled


In Oncology, Vaccines,
Medical devices


FDA and EMEA submissions

Portfolio of services delivered

  • 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


  • DMC/DSMB services

Case Study

Learn more about how our team helped navigate a complex ISS/ISE submission


Download to learn how our biometrics solutions can help you augment internal expertise and capacity in record time

Why Algorics?