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.