Compliance

Medizap Compliance

COMPLIANCE

MediZap offers support, guidance and best practices for each of its customers in the context of 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 operations.

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

MediZap leverages direct contact with regulatory agencies (FDA, DEA, ISO, and State Pharmacy Boards), industry conferences (IACP, A4M World Congress, IMCAS and PCAA), online research and exclusive partnerships to constantly learn and evolve knowledge regarding sterilization services for compounded pharmaceutical products.

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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