A well-defined regulatory plan and strategy is essential to obtain the marketing authorisation and put a product into market as quickly as possible. Once a marketing authorisation or CE marking is obtained, it must be maintained up-to-date and reflect changes in manufacturing, risk-benefit balance and any changes in legislation.
Our team has extensive experience in the regulatory steps and development paths required for medicinal and health related products.
We support our customers with distinct collaborative approaches, from personalised expert support to in-company employee training.
Registration of medicinal products and
Review of promotional
Auditing and consolidation
of registration dossiers
Our team is made up of experts with extensive experience in multiple types of product: