Scaling from Milligrams to 1–2 kg

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The aim of the course is to provide attendees with a good basis to work from when involved in taking development candidates to the first in human trials with a view also on some longer-term requirements. The course content will therefore focus on the necessary early phases of chemical development as would typically be required to support production of up to about 2 kg using laboratory-based 20 L glassware.


Tutor

  • Dr. John Knight


Topics

  • Requirements in order to move from small (less than 1g) supplies to the first 100g or so for preclinical work
  • Further scaling to 1-2kg non-cGMP
  • Requirements to make material for use in clinical trial – an introduction to cGMP coupled with the scaling issues
  • An overview of the requirements to move processes to fixed vessels, assuming cGMP is required – what operations can readily be transferred and those that should ideally be developed out
  • The phases of development and indicative timelines with quality requirements
  • The importance of physical form selection, understanding and control
  • Impurities and their control, with specific discussion on genotoxic impurities and developing the specification for the API as it moves from preclinical batch preparation to cGMP batches for clinical trials


Who Should Attend

  • Project managers and those involved in technical outsourcing
  • Project leaders and bench chemists involved in preparation of material
  • New starters to the area
  • Medicinal Chemistry support teams involved in making the first batches for toxicological evaluation

 

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