At Formulife, quality is proven at every stage of our supplement manufacturing process via in-house and third-party laboratory verification. Our rigorous, full-spectrum QA prevents costly issues, and elevates your customer experience.
Need a quality-first team ready to nail your deadlines? Build and launch at speed with Formulife’s in-house laboratory and full-time team of chemists and microbiologists.
From our first contact with a supplier to the shipment of your finished product, Formulife adheres to a industry-leading 3-stage QA process that ensures the reliability of every aspect of your product across every single run.
All raw materials are pre-vetted and verified prior to purchase. Incoming materials are quarantined and thoroughly analyzed on arrival to our facilities.
In-process formulation samples are tested for consistency with your past runs, so that any potential issues can be detected and corrected immediately.
Finished-product testing certifies that all QC requirements are met, resulting in the best possible experience for your customers.
Exceptional quality begins at the source. Other manufacturers may choose suppliers with material variability that can negatively impact your product consistency and customer experience. Formulife’s deep network of vetted suppliers sets you up for superior reliability, and consistently stellar products.
FOURIER-TRANSFORM INFRARED SPECTROSCOPY
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY
STATE-OF-THE-ART MICROBIOLOGY TESTING
INDUCTIVELY COUPLED PLASMA-MASSSPECTROSCOPY
Thin layer chromotography
We identify the unique infrared spectrograph “fingerprint” of your product via FTIR testing. This allows us to match and confirm the continuity of your product at each stage of product, across all production runs.
Our lead Quality Control staff verify the taste, smell, and visual appearance of your product of dry form and in solution, if applicable.
We verify with quantitative analysis one active ingredient in your finished product via HPLC, GC, or ICP-MS instrumentation.
Our in-house lab tests for the presence of lead, cadmium, arsenic, and mercury via ICP-MS machines.
Solid-dose products are tested for consistency in weight.
State-of-the-art automated microbiological testing is performed on every batch. Tempo® testing identifies and quantifies YM (yeast and mold) and APC (aerobic platelet counts). Gene Up® real-time PCR testing detects pathogens (E. coli, Salmonella, and Staphylococcus aureus).
Get peace of mind with facilities and processes that are independently reviewed, and receive comprehensive third-party certifications. All of our manufacturing processes meet or exceed GMP standards.
We’re premium. We developed a brand and products that resonate with our customers. If we’re going to hand a project over to a manufacturer, it better meet those expectations. With Formulife, we can scale without sacrifice. They’re hyper-customer and quality-focused.
Other manufacturers make short-term material decisions based on cost and availability. But these shortsighted choices can easily lead to inconsistent products with a mediocre customer experience.
Formulife takes a customer-first approach. We leverage every aspect of product quality throughout our process to deliver superior material, taste, smell, visual, and experiential reliability.
As our 15 years of supplement manufacturing expertise have proven, a consistently standout experience leads to increased LTV.
Choose quality where it counts… and watch the results compound.
Don’t take risks with short-term manufacturing choices that can undercut product quality. Get the high-caliber experience that will thrill your customers, and keep them coming back.
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Formulife LLC
1253 Andrews Pkwy, Allen, TX 75002
(214) 221-4911
These statements have not been evaluated by the food and drug administration. These products are not intended to diagnose, treat, cure or prevent any diseases.