Regulatory affairs
Local representative of the Marketing Authorisation Holder
A marketing authorisation may only be granted to an applicant established in the European Community (Art 8 2001/83/EC). Furthermore, some member states require a local representative be appointed and included in the contact details of the Patient Leaflet. DADA has the required legal entities and organisation in-house to act as your European Community establishment and/or as local representative in the Netherlands, including liaison with health care professionals or the public in the local language, handling of product questions or complaints, and more.
Services
Other services in Regulatory affairs
- Early Access programs
- Health-based exposure limits (HBEL)
- EU language translations
- PIL user testing
- Certificate of a Pharmaceutical Product / Free sales certificates
- Reimbursement applications
- Appeals and hearings
- Due diligence and in- and out-licensing support
- Organisational advice
- Scientific advice
- Feasibility studies
- Regulatory strategy
- Marketing authorisation applications
- Marketing authorisation dossiers and maintenance
- Expert reports, overviews and quality overall summaries
- Program and project management
Business hours
- Monday – Friday
- 9am – 5pm
- Saturday
- Closed
- Sunday
- Closed