Regulatory Affairs
Official authorizations and submissions are a global obligation for manufacturing and distributing pharmaceutical products and medical devices. This often means a significant requirement for resources and know-how on the part of the companies who need to meet the requirements.
Dr. Notghi Contract Research GmbH has experienced and dependable experts in this field.
We help you conserve your valuable resources and reduce costs.
Strengths
- experiences in exposure to regulatory affairs
- multilingual and qualified personnel
- interdisciplinary resources and expertise are flexibly available
Dr. Notghi Contract Research GmbH offers you a wide service range for Regulatory Affairs with full and partition service solutions.
Services at a glance
- consulting and supporting with authorization and admission procedures
- preparation of petitions and reports for regulatory purposes
- implementation of legibility-tests
Our experts will gladly provide you with personal consultation. We look forward to hearing from you! Contact