Blogs #GMP
Quality Assurance (QA) vs. Quality Control (QC): Understanding their 9 Crucial Contrasts in Pharmaceuticals and Medical Devices
Quality in regulated industries refers to the degree to which a product or process meets predefined standards and regulatory requirements.
What is the Difference between GLP and GMP Testing Regulations?
GLP and GMP are at times confused as the same as it pertains to Laboratory testing. It is understandable that both cover Lab Testing still are different. Knowing the difference becomes very important here.
What is the Difference between GLP and GMP Testing Regulations?
GLP and GMP are at times confused as the same as it pertains to Laboratory testing. It is understandable that both cover Lab Testing still are different. Knowing the difference becomes very important here.
How does FDA classify medical devices?
In accordance with the Federal Food, Drug, and Cosmetic Act, FDA places all medical devices into one of three regulatory classes based on the level of control necessary to ensure safety and effectiveness of the device