Remediation Consulting, LLC applies specialized programming using the "Guidance for Industry, Q7A - Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients", and FDA's Compliance Guidance Manual 7356.002F.  These references, and other related regulatory standards (e.g. OHSA, EPA, DOT), are the background for optimizing the manufacture of active ingredients, as well as excipients, catalysts and additives.   

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High quality / low cost starting materials result in more reliable, safe and effective finished products.  Remediation Consulting, LLC understands that raw material manufacturers supply a variety of diverse clientele with different specification criteria for the same material. We assist companies in managing this opportunity with flexible and cost-effective solutions, to serve this common occurrence.

 

"Living organisms are created by chemistry. We are huge packages of chemicals."  -   David Christian