Pharmaceutical

High Force Research has an enviable, 30 year track record of delivery in the area of chemical and pharmaceutical industries.

We have been inspected by the MHRA and are in compliance with the principles and guidelines of good manufacturing practice as regulated by ICH Q7 and Eudralex volume 4 part II for clinical trials.

Our facilities include two segregated ISO Class 8 laboratories in which multi-stage synthesis to cGMP standards is carried out. Each facility operates at a 30 litre scale, typically enabling production in batches of up to multi kilo quantities

The work we do for clients is aimed at optimising route design leading to:

  • development & optimisation
  • improved yields
  • process step reduction
  • reduced batch cycle times
  • elimination of hazardous materials
  • a scalable process for taking through to clinical trials
  • analytical development