Rechon have experience in the manufacturing of clinical trial materials for all stages of clinical development.

 

Our services include:

  • * Clinical manufacturing, phase I, II, III and IV
  • * Import of clinical trial supplies
  • * Labelling, packaging, blinding and distribution to clinical sites worldwide
  • * QP and “Green card” release
  • * Regulatory support documentation (CMC/Module 3)
  • * IND and IMPD documentation

 

Rechon can manage the entire clinical supply chain from manufacture through transport to clinics, returns and destruction.