Welcome to cr.appliance
We support drug development activities by our clients through
- our high-quality independent consulting services and by evaluating and augmenting development concepts,
- our flexible, reliable, high quality service,
- our successful international experience in regulatory processes,
- our proven partnerships with study centres, investigators, CRO partners and academic institutions,
- our work in clinical and regulatory networks.
We have supported companies in the healthcare industry in the development and registration of drugs for the last seven years. The clients we have helped particularly appreciate the specific expertise of cr.appliance in the fields of human pharmacology, experimental medicine, early clinical development to “proof of concept” and the preclinical/clinical interface.
Our advice and services are sought on a wide range of issues and challenges in early clinical development, including support and planning for biopharmaceutical development projects, providing additional external expertise during the submission and licensing process, and on life cycle management issues.