| Comment Record |
|
Commentor |
Dr. Richard Tseng |
Date/Time |
2003-03-17 12:10:33 |
|
Organization |
Pharmanex |
|
Category |
Dietary Supplement Industry |
| Comments for FDA General |
| Questions |
|
1. General Comments
|
The newly proposed cGMP for dietary supplement does not include a raw material retest program. For those raw materials which can not be used up in a short time, should they be tested at least at yearly basis to ensure their quality (potency, water content, microbial contamination, etc)?
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