New GMPs Make Product Testing a Key Factor in Manufacturing
The new rules and regulations under the GMPs range from tighter manufacturing practices to detailed documentation, new personnel regulations, and detailed product testing. Raising the bar on quality manufacturing will, no doubt, serve to enhance the image of the supplement industry.
Why GMP is so important ? A consumer usually cannot detect (through smell, touch, or sight) that a drug product is safe or if it will work. While GMPs require testing, testing alone is not adequate to ensure quality.
Product Testing and the GMPs
In the past, the emphasis on product testing was on the finished product. Under the new GMPs manufacturing facility, however, testing is used as a means of quality control. It begins before manufacturing with detailed documentation of finished product specifications, manufacturing processes, and process controls and tests that would be used to ensure reliable results.
GMP-Certified Manufacturing Facility One sure way such, FDA registered manufacturers can keep their products flowing in the market is through contract manufacturing with private label supplement manufacturers that have a fullyequipped lab with analytical equipment and a GMP-certified facility. A&C is a global GMP manufacturer of excipients, buffers, process solutions, and a select number of active pharmaceutical ingredients (APIs).
Besides superior-quality GMP manufacturing facility is a service-driven organization to find unique solutions to our customers’ GMP challenges. We are a privately owned company where flexibility, transparency, and quality are at the core of all of our activities. This is demonstrated through the numerous quality certifications that A&C holds: ISO 9001:2015* EXCiPACT GMP and GDP for excipients Drug Establishment Licence for the manufacture of APIs FDA and Health Canada audited
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