Welcome

IBB Consulting supports players in the pharmaceutical drug development arena with

  • the design of non-clinical safety programs,
  • outsourcing and monitoring of non-clinical safety studies,
  • interpretation of toxicology data
  • and the generation of regulatory submission documents.

Pre-clinical Safety in Drug development

We help you with

Advice - Planning - Outsourcing - Evaluation

of your Non-Clinical Safety Program  

NON-CLINICAL SAFETY PLANS


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STUDY CONDUCT and CRO OUTSOURCING


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REGULATORY and SCIENTIFIC DOCUMENTS


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EDUCATIONAL SESSIONS


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Together we bring safe medicin

to your patients

Ingrid Brück Bøgh      *      Mobile: +45 5383 6655      *      Email: ingrid@ibbconsulting.dk        

Copyright © All Rights Reserved  -  Ingrid Brück Bøgh   + 45 5383 6655  -  ingrid@ibbconsulting.dk