With more than twenty-five years of experience as a global company, we at Magid-Haffner have associates that have regulatory expertise in the EU, US, Japan, India and China for Pharmaceutical, Biotech and Medical Devices

We provide the following services:

  • GMP consulting services
  • FDA and EMEA submissions
  • GXP Training programs
  • FDA Pre-Approval (PAI) mock audits
  • SOP writing and documentation review
  • Deviation and CAPA investigations