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Why

I assist the Pharmaceutical, Biotechnology, and Medical Device industries meet their patient's, company, and global regulatory needs by providing consulting and auditing services to meet Quality Management System (QMS), Good Manufacturing Practice (GMP), and Good Distribution Practice (GDP) requirements. I keep your patient's lives in mind. As a team, we collaborate to determine what's best for your patient's and your company.
Melissa Hyatt

I've been conducting global audits for over 20 years evaluating compliance to domestic and international regulations.
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Federal Regulations: Health Canada, Japan, MHRA, ANVISA, FDA, EMEA
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International Standards: ISO 9001, ISO 13485, ISO 14001
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USP <795>, <797>, and <800>
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I'd appreciate the opportunity to assist your team in meeting their goals!
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