CKALITA CONSULTING brings you all the expertise in QUALITY - REGULATORY -BUSINESS DEVELOPMENT in the LIFE SCIENCES EMA-FDA: Pharmaceutical Industry, cosmetics & Medical Devices.

We will help your teams for any cGMP- GMP- GLP- GDP and GCP project

  • QUALITY :  CDMOs & suppliers qualification – Audits- FDA Mock inspections training- Quality Systems & Documentation Management.

  • REGULATORY : CMC writing - IMPD/IND- QP training & replacement.
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  • BUSINESS : Start-ups & companies development – Project Management
    - Managers freelance transitions- Products Life Cycle management