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You've probably noticed;
ordinary companies don't create extraordinary products.

They lack the science. They lack the talent. Most of all, they lack the imagination. At Lunada, you'll find innovative technology and visionary thinking at every phase of product development. These traits have helped us create the first really new line of anti-aging products in a long time. The science behind our formulations is based on a technology no other company can offer.

We pioneered it. We perfected it. And now we're using it to offer exclusive anti-aging formulations with the power to rejuvenate from within.

Before any Lunada product is released, it must first stand trial.

Our product development process is unrivaled in the natural health industry. From initial inception to finished formula, every phase of development is scrutinized. As shown below, our gauntlet of tests, evaluations, and screenings is brutal. But it's the only way to ensure that the finished product you receive delivers the highest levels of safety, quality, and efficacy.

1

Pre-Testing Research



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All new formulations begin with a search. We start by looking for the specific mechanisms of disease or aging. Then we identify beneficial compounds that can alleviate these mechanisms.

2

Extraction and Synthesis



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Once we've isolated a beneficial substance, we scour all available sources of this compound and test each source in our laboratory. Our goal is to find the source of active components with the highest level of quality and effectiveness. If the best raw materials fail to meet our standards, we'll engineer ingredients with even higher biological activity levels. If all substances fail to address our needs, we'll attempt to synthesize our own compounds in the laboratory.

3

Screening and Testing



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Having acquired the best compounds, our next step is to assess their biological activity and therapeutic merits. This phase involves a full barrage of tests: we conduct animal studies, examine isolated cell cultures and tissue cultures; we perform enzyme studies, evaluate cloned receptor sites and analyze computer-modeling studies.

4

Dosage Formulation
and Stability Testing



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Here, we determine the optimal form in which to deliver a compound. Our active ingredients can be formulated as tablets, capsules, liquid, powder, ointments, sprays or patches. We also determine the ideal dosage strength for human use.

5

Toxicology and Safety Testing



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Before a Lunada compound is ever tested on humans, it must first pass a full spectrum of safety tests. These include toxicology evaluations, animal studies, tissue cultures and other testing studies. During this phase, we compile data on the compound's dose-response patterns and look for any possible side effects or toxic effects.

6

Human Clinical Trials



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Lunada Biomedical conducts all clinical trials in accordance with the principles of evidence-based medicine. We use randomized, crossover, double-blind and triple-blind methods of control. These trials define the compound's pharmacologic effects at anticipated therapeutic levels, and provide valuable study data on absorption, distribution, metabolism, and excretion patterns in humans.

7

Data Analysis



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All results of clinical trials are processed and thoroughly analyzed. Our research staff evaluates a number of different areas, including quantitative assessment of effectiveness based on established mathematical models.

8

Manuscript Submission
and Review



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Like all evidence-based research companies, Lunada openly shares new data gathered in clinical trials through the peer-review process. Clinical trial manuscripts are prepared and submitted to appropriate peer-review publications. This process encourages an open dialogue between Lunada researchers and other top minds in the biomedical field.

9

Product Launch



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Once the studies are published in a peer-reviewed publication, our new product is ready to be introduced to our customers.