Compliance

Medizap offers guidance, support, and best practices for each of its customers in document control and compliance. We are an extension of your quality control and quality assurance teams so that you can feel confident in your sterile compounding and drug manufacturing operations.

With compounding pharmacy, outsourcing facility, and pharmaceutical company customers across North & South America, we have the benefit of engagement across the industry and the ability to cascade insights to our customers to keep them one step ahead in the compliance game.

MediZap leverages direct contact with regulatory agencies:

  • Food and Drug Administration
  • Drug Enforcement Agency
  • State Pharmacy Boards
  • United States Pharmacopeia
  • International Standards Organization

MediZap participates in industry conferences:

  • Alliance for Pharmacy Compounding
  • American Academy of Anti-Agency Medicine
  • International Master Course on Aging Science
  • Professional Compounding Centers of America

We support your document control needs and preparation for regulatory audits. Medizap provides consolidated industry information and an additional knowledge source base for compliance advisement so that you can focus on what you do best.


"WHEREVER POSSIBLE, HEALTHCARE PRODUCTS INTENDED TO BE STERILE SHOULD BE STERILIZED IN THEIR FINAL SEALED CONTAINER (TERMINAL STERILIZATION)."
-ISO 13408-1


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