The U.S. Food and Drug Administration (FDA) established strict rules for businesses involved in the production, packaging, labeling, and holding of dietary supplements in its final regulation on good manufacturing practices (GMPs) for such products. Manufacturers must assess the identity, purity, quality, potency, and formulation of their dietary ingredients in accordance with the Dietary Supplements GMP. GMPs are essential to the supplement industry’s ability to provide consumers with safe, precisely labeled goods and maximize the benefits for public health.

GHP provides GMP consultant services to assist its clients with procedures that let them create high-quality products with effective, GMP-compliant operations that reap benefits even after the project is complete.

GHP as a GMP consultant has supported the pharmaceutical industry for many years with a broad range of services. We are based in the US and offer services that connect pharmaceutical businesses to the FDA’s regulatory framework in a number of countries.

GHP works with a diverse network of consultants on a global scale to deliver the required diversity and quality of our services. To give our clients the advantages of a cost-effective engagement and the best and most competent consultants available for the specific task at hand, we may staff our projects with a combination of multinational and multilingual specialists and technicians. We can communicate in a variety of languages with clients and regulatory bodies.