Our expert and scientific teams combine a solid experience of the development and regulatory affairs and offer to assist in the following areas:

Consulting in pharmaceutical development

  • Assistance in preparation of the development plans
  • Writing of study protocols

Formulation and analytical expertise

  • Audit of pharmaceutical dossiers (product acquisition, update of dossier, variation..)
  • Expert reports
  • Troubleshooting

Consulting service for veterinary preclinical and clinical development

  • Veterinary healthcare product development strategy
  • Writing of study protocols
  • Audit of dossiers
  • Expert reports

Consulting and assisting in Regulatory affairs

  • Technical, scientific and regulatory assistance for the pharmaceutical part, in conformity with current regulatory requirements.
    > read more

GMP auditing - Europe and ROW (in partnership)

  • API manufacturers
  • Finished Products manufacturers