Consultancy

Kantisto covers all phases of drug development, from discovery and early phase up to late phase development, marketed product support and line extensions. Kantisto can support you with practical technical issues, Quality by Design and also with documentation for regulatory approval such as IMPD/IND and MAA/NDA. There is a long experience with quality systems such as GLP and GMP. A focus on knowledge transfer and implementation means that Kantisto prefers to work not just for you, but with you on-site, in close cooperation and collaboration, with a pragmatic scientific and personal approach.

  • Scientific and managerial coaching
  • Technical coaching, training and workshops
  • Implementation trajectories of instrument and technique
  • Good working practices
  • Method scouting
  • Method and application development, validation and transfer
  • Quality by Design QbD
  • Reviewing and writing CMC and other regulatory documentation
  • Troubleshooting and application improvement
  • Pragmatic quality systems, GLP, GMP