The FDA has adopted GMP regulations that apply to all phases of dietary supplement manufacturing, distribution and sales.
GMPs require manufacturers to establish specifications for the dietary ingredients and dietary supplements they produce.
Standard operating procedures (SOPs) in critical areas of cGMP compliance should be in place at all phases of product development, manufacturing and distribution.
Is your company doing actual testing for ingredient identity to comply with the new FDA requirements for GMP?
AER IS HERE
All serious adverse events must be reported to the FDA. Are your ready?
cGMP REQUIREMENTS
The rules apply to you even if you use contract manufacturing. Do your SOP's measure up?
CLAIMS DEVELOPMENT
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