Welcome to the leading Regulatory Affairs consultancy
A regulatory strategy and a well-defined plan are essential to obtain the authorization to modify a product and take it to the market as quickly as possible.
At Azierta, we are experts in Regulatory Affairs and adapt to the needs of our clients to require the success of their projects.
We support our customers with distinct collaborative approaches, from personalised expert support to in-company employee training.
Our regulatory strategy services in the Pharma sector:
- Medication registration and maintenance
- Review of promotional material
- TAC service (Marketing Authorisation Holder Service)
- Auditing and consolidation of registration dossiers
- eCTD (update to European regulations)
- Regulatory support through "implants"
Our team is made up of experts with extensive experience in multiple types of product.
Specialized in multiple types of products: