Toxicology Consultant with >25 years of experience in the Biopharmaceutical Industry. I support 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
- +41 78 622 46 88
- Send an email
- Jörg Herbst