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      Manufacturing to a Higher Standard

      These days, most dietary supplement companies are really sales and marketing firms. While they may formulate their own products, it is standard to outsource the manufacturing, laboratory testing, bottling, and labeling to a big contract manufacturer. The upside to this practice is that it’s convenient. The downside is that companies lose control to others that don’t share the same passion for the quality of the products.

      Revive MD Products are unique in that we operate our own 100,000-square-foot, cGMP, FDA-audited manufacturing facility that is based in Stevens Point, Wisconsin and staffed by highly trained personnel who share a passion for efficacy. Because we control the entire production process — from formulation…to raw materials sourcing…to manufacturing…to laboratory testing of incoming materials and finished product…to bottling and labeling — we are free to be perfectionists.

      Our manufacturing facility is strictly controlled by rigorous standards that meet cGMPs, and it routinely passes FDA and third-party audits. Extensive testing on every product we manufacture means you can trust the consistent purity, strength, identity, and composition of each and every Revive MD's Products formula.

      It’s rare for a supplement company to handle all phases of production. But when your standards are as high as ours, you don’t want to entrust it to anyone else.
       

      Quality Beyond What's Expected

      It is an understatement to say that there is wide variation in quality
      among dietary supplements.

      How many times have you read a news report revealing that a shocking percentage of products tested contained only a fraction of the ingredient potency they claimed to have…or a newspaper story about a supplement that was contaminated with heavy metals, or worse, adulterated with cheap material?

      Following are just some of the steps Revive MD Products takes to ensure the quality of our formulas:

      • We follow rigid SOPs (standard operating procedures) and MOPs (methods of procedure) throughout every stage of production, leaving nothing to chance.
      • We test all incoming raw materials in our state-of-the-art, in-house laboratory for identity (Is the material what it says it is?), purity (Does it contain any contaminants?), and composition (Does it match expected specifications?).
      • We mix all of our raw materials in dedicated blending rooms using a custom-made 5,000-liter mixer following strict protocols to ensure product consistency.
      • We manufacture every batch of product in dedicated tabletting and encapsulating rooms, which are thoroughly cleaned and dried after each batch is made to protect against cross-contamination. It can take up to eight hours just to clean one room!
      • We perform thorough post-cleaning inspections to ensure the highest state of sanitation has been achieved.
      • We test all finished products for identity (Does the formula contain the correct ingredients?), strength (Are the ingredients present in the potencies claimed?), and purity (Does the formula contain any contaminants?).
      • We subject every new formula to stability testing, which involves assaying ingredients to detect any degradation at 6-month intervals, thus ensuring the formula meets label claim at expiration.