Regulatory approvals and permits are required for the manufacture and distribution of medicinal product almost worldwide.
For companies, that often means a high expense of resources and expertise in order to meet the statutory requirements. For you as a pharmaceutical company, this often means a strong personal commitment in ensuring the regularity towards the authorities.
We have experienced and reliable resources in this area.
What we offer in Regulatory affairs:
- Advice and support in approval and licensing procedures
- Preparation of proposals and reports for regulatory purposes
- Carrying out readability tests
You benefit from:
- experiences in exposure to regulatory affairs
- multilingual and qualified personnel
- interdisciplinary resources and expertise are flexibly available
We offer a wide range of services in the field of Regulatory Affairs with full and partition service solutions.
Our experts will gladly advice you personally. We look forward to your call or your message.