21 CFR 211 Subparts J & K: Records and Salvaged Drug Product

Most industries in the US are regulated by local, state, and federal regulators and pharmaceutical manufacturing companies are some of the most highly regulated, particularly at the federal level. Pharmaceutical Quality affects every American hence the FDA regulates the quality of pharmaceuticals very carefully. The main regulatory standard for ensuring pharmaceutical quality are the Current Good Manufacturing Practice (cGMPs) regulations.

This 90-minute Accredited Course will discuss the FDA regulations 21 CFR Subparts J&K addressing the words and meaning as they apply to the USA Pharmaceutical Industry. The course will show how these paragraphs are to be interpreted and how one should comply. 

THIS TRAINING IS PART OF OUR GMP PROFESSIONAL CERTIFICATION

• To enroll into the complete GMP Certification Program CLICK HERE.  This program includes 10 specific online courses for $2050.
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