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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.

80

+

Biostatistics and programming staff

95

+

Studies delivered to date

20

+

DMCs handled

Experts

In Oncology, Vaccines,
Medical devices

Successful

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

  • 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

Why Algorics?