Slide We deliver rapid, guaranteed results that make the most of every datapoint, helping clients move rapidly through research and development to market approval. Quantics is a biostatistical solutions provider for the bioscience and medical devices industries.
  • Bioanalytics / Bioassay

  • Clinical Biostatistics

  • Medical Device Studies

  • Health

  • Vaccine Development

  • GLP Compliant Analysis

  • GMP Compliant Analysis

  • Training

  • QuBAS -
    Bioanalytical /

  • QcBOT

  • CrtV

Bioanalytics / Bioassay

Design, optimisation, validation, and routine analysis for bioassay and bioanalytical projects


We deliver rapid, guaranteed biostatistics that make the most of every datapoint

Clinical Biostatistics

Biostatistics supplier to the world's largest CROs

Medical Device Studies

Class I-III, including diagnostics, and wearables. Experts in study design including efficient adaptive trials.

Health Technology Assessment

From simple meta-analysis and network meta-analysis to complex population adjustment methods such as MAIC and STC.

Vaccine Development

Correlates of Protection, Time-to-event and Passive Transfer analysis for complex therapeutic and biodefence vaccine development programs.

GLP Analysis

Rapid turnround GLP certified statistical analysis of tox and ecotox studies according to OECD and other regulatory guidelines.

GMP Analysis

Rapid turnround routine GMP statistical analysis of batch release and other GMP analyses.


Virtual and onsite training for scientists, covering introductory and advanced statistics for bioassays and Network Meta Analysis used in HTA.

QuBAS - Bioanalytical / Bioassay Software

Bioassay software for development to routine GMP with industry changing CrtVTM technology that is FDA CSA ready.


Systems that automate manual import/export of data in regulatory environments. Incorporating CrtVTM technology – FDA CSA ready.


Continuous real-time Validation is an automated approach to validation processes deployed across Quantics including QuBAS and QCBOT.

Customer Feedback

Slide Using a mathematically efficient approach for LD50 and vaccine challenge assays can reduce animal numbers required per assay by 30% or more, resulting in major cost and time savings, and requiring no change in laboratory techniques.

Save money, save time, save guinea pigs.
Survival Analysis FIND OUT MORE

Slide Did you know you could cut out QC on data transfer between systems with Continuous real-time validation (CrtV)?

CrtV is a process of 100% in-use testing of data that can be applied to any situation where there is cut-and-paste with or without simple data analysis.
CrtV: A Brief Explanation FIND OUT MORE

Slide To find the most effective and safest treatment for a disease, potential treatments must be directly compared.

Network meta-analysis provides an ideal statistical method to simultaneously compare any number of treatments in order to find which is best.
Network Meta-Analysis FIND OUT MORE

Slide QuBAS is a feature rich statistical analysis software package with all of the commonly used statistical methods for relative potency and ELISA assays.
QuBAS Bioassay Software FIND OUT MORE

Our Support



Quantics work to full regulatory compliance

Customised Service

Fast, reliable service customised to your needs

A Unique Company

A Unique Company

Unique in having ISO9001 and MHRA GLP Test Facility certification

100% Independent

Quantics can provide a completely independent service

Excellent Reporting

Presentation of results aimed at non-statistical audiences

Optimal Statistical Techniques

Optimal Statistical Techniques

Exploring and developing new approaches to difficult analysis problems

Experienced Team

Quantics employs highly experienced and qualified statistical, scientific and medical staff

365 Days

Providing a personal statistics service every day of the year

Learn about how we optimise experimental and analytical design in bioassay to help secure FDA approval


GMP or GLP Routine and Bespoke Statistical Analysis Service

Process Support

Full process control support / trending if required

Same Day Reporting

Same day draft reporting for routine GLP & GMP statistical work

QA Report

2 days, ready for use QA report for all GLP & GMP routine work

QC Check

Guaranteed 100% QC check of every result

365 Days

Providing GLP & GMP Statistics all year round