Toxicologist consulting for the Biopharmaceutical Industry and supports Startup and Biotech Companies to advance their projects into the clinical phase. Get in touch to discuss your project when you have a shortage of nonclinical and toxicological expertise.
Products, services, technology
Nonclinical Development Plans - Regulatory Writing (Briefing Books, Submission Documents) - Safety Assessments (Leachables, Excipients, degradation products) - Risk Benefit Assessments - Justification Documents and waivers - CRO Selection, Study Management and Study Monitoring
- http://www.ncma-consulting.com
- +41786224688
- jherbst@ncma-consulting.com
- Jörg Herbst
