DIA Europe is the must-attend event for all life science professionals working in drug development, from discovery to marketed use.
Azierta, as a consulting firm specialised in science and health, provide a complete solutions throughout the products’ life cycle, such as:
- Full Regulatory Affairs and Pharmacovigilance Support
- Vigilazierta Pharmacovigilance Expert Database
- Quality Assurance
- Medical Cannnabis Consultancy
- REACH Compliance Support- CLP & Biocides
- Toxicology Support
- European Market Access Support Services “EU-GMP Certificate”
Contact us to schedule a meeting with our experts:
Eduardo Rodenas Rocha
Chief Scientific Officer
Pharmacovigilance Science Manager
Regulatory Affairs Business Office Director
Chief Communication & Marketing Officer
Start creating your itinerary and don't forget to add our session on Thursday 18th at 2.00 h PM with Silvia de Andrés as main speaker, Eduardo Rodenas Rocha and Aintzane Goicoechea.
“Monitoring and Surveillance in the Marketing of Medical Devices”
Impact of the pandemic on Medical Devices
New vigilance requirements
PSUR and PMS reporting
Post-market clinical follow-up
Silvia de Andrés
Medical Devices and Vigilance Officer
If you are not able to attend the event, and would like to receive the contents of the session, please click here and request it!
*The content will be sent to you once the session is over.