Estroven’s Commitment to Safety & Quality
We are proud of our menopause and perimenopause products and how well they work. Every Estroven production run undergoes a great deal of testing for purity and potency. These tests are performed by qualified laboratories, which follow standards set by various scientific agencies, including the U.S. Food and Drug Administration (FDA), U.S. Pharmacopeia (USP), NSF, AOAC, and other internationally recognized standard-setting authorities.
We have developed a strict set of standards for the vendors who supply our ingredients and products. All suppliers must follow current Good Manufacturing Practices (cGMPs) established by the US FDA. All dietary ingredients are tested for identification and to ensure they meet pre-set specifications. We audit all facilities and operations to be sure they meet current good manufacturing standards. We constantly exchange information with our vendors, so that we can keep improving our process.
Qualified analytical testing laboratories test all batches of Estroven for potency so that our products can be correctly labeled. Proprietary blends of herbs cannot be tested by traditional methods; therefore, product specification standards are used and verified through thorough review of the batch documentation. We have standard operating procedures for:
It is essential that the quality of our products does not lessen over time, and that they are as effective from the day they leave the plant to the day you purchase them. For this reason, we make sure that they meet expiration date requirements, so whether you use the product the day it is made or at the end of its shelf life, it delivers what we promise. Annual stability testing is a standard process for Estroven.