Meticulously coordinated processes contribute decisively to the success of your development projects.
The profound experience of the s4s team offers precisely coordinated and reliable handling of your workflows in the external performance of projects:
Our role can be planned accurately within your overall project - transparently and comprehensibly down to the last detail.
s4s takes over:
- Accomplishment of approval procedures and maintenance
- Any pharmacovigilance activities required
(with our own pharmacovigilance system in accordance with EU and German requirements) - All the documents required for drug development, approval and pharmacovigilance
- Regulatory affairs documentation for veterinary drugs
- Expert reports, Medical writing
- Literature research, data analysis
- Dangerous goods classification, technical documentation
- Project management for studies
- Consultation in our areas of competence
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