TRAINING

RenaClinical's external training program is run and managed via their QPs.  Training can be tailored to the needs of the client in order to achieve the best possible outcomes.  On-site and remote training packages are available to all clients.  Training certificates can be issued to document all training and CPD events.  

Onsite classroom based training and tutorials, online webinars and support packages available for all RenaClinical clients.

Recently completed training packages:

  • The Impact of Brexit to Clinical & Commercial Supply Chains

  • Introduction of the EU Clinical Trial Regulation

  • ATMP De-centralised Manufacturing

  • Role of the QP in Clinical Trial Manufacturing & Distribution

  • Regulatory and GMP requirements of NIMPs

  • Supply chain and Transportation Risk Assessments

  • EU Importation of IMPs

  • Impact of FMD to Clinical Trial Supply Chains

  • EU Pharmaceutical Legislation (Delivered to Chinese FDA Inspectors)

Training has been provided to the following client base:

  • Clinical Trial Units

  • NHS Hospital Pharmacies

  • Researchers

  • Principal Investigators

  • Manufacturing Organisations

  • Regulatory Consultants and Universities