Our experts in vector-borne diseases, vector biology and vector control, who hold significant experience working in the laboratory and field, can offer oversight and insight on everything from research and development, right through to product registration, dossier submission and full field evaluation.

Product development

Our team of world leading entomologists and clinical trials specialists offer insight and advice on a wide range of areas for product development and evaluation, including:

  • Generation of ideas and innovations to solve a particular problem, or address an unmet market need
  • Active ingredient guidance
  • Strategic research and development programmes and planning
  • Study design, preparation of protocols, risk assessments, data analysis and data interpretation
  • Review of scientific proposals and literature
  • Review of company policies and Health and Safety materials relating to public health risks
  • Efficacy testing for product development and registration
  • Good Clinical Practice (GCP) and Good Laboratory Practice (GLP)

On-site monitoring
and quality assurance

Our experienced clinical trial managers and research entomologists offer independent monitoring and oversight of laboratory and field intervention trials (Phase I, II and III) and Good Clinical Practice (GCP).

We can develop and conduct bespoke monitoring programmes for laboratory and field trials, as well as conduct site visits to ensure quality assurance.

Product registration

We offer clients regulatory navigation through, and regular dialogue with, national regulatory bodies such as the Medicines and Healthcare Products Regulatory Agency (MHRA), local NHS Ethics Committees, the Health and Safety Executive, and compliance with the Biocidal Products Regulations and also international bodies such as the Environmental Protection Agencies (EPA) for the US and Australia.