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.