“When we engage with a client to manufacture their products it is highly likely that the end product will exceed the performance of the original formulation presented to us.”
The team at Life Factor Research is responsible for manufacturing high quality nutraceutical products using a variety of facilities, technologies, delivery mechanisms and any other metric of consequence for the past thirty plus years. During that time LFR has garnered the experience, knowledge and perhaps most important correct relationships to guarantee the outcome prior to starting the project. When we engage with a client to manufacture their products it is highly likely that the end product will exceed the performance of the original formulation presented to us.
Delivery and Absorption
At LFR we consult and advise all of our manufacturing clients as to which of our proprietary absorption technologies will provide the end user the best possible value and outcome by insuring maximum delivery of actives to the blood stream.At the same time, we will discuss delivery mechanisms such as tablets, capsules, powders, drinks, sublingual strips, and the list goes on. LFR has the ability to incorporate these two key elements in each and every product or product line that we work with which will greatly effect the overall performance of the end product, distribution and sales.
Nutritional and nutraceutical product quality affects every American consumer.
The Food and Drug Administration (FDA) inspects and evaluates the quality of every manufacturing facility very carefully. The primary standard for ensuring quality is the Current Good Manufacturing Practice (CGMPs) regulation.
Consumers have the right to know that every product from any batch of product they take will meet quality standards so that they will be safe and effective. Many are not aware of cGMPs, or exactly how FDA assures that manufacturing processes meet these basic objectives. Our Life Factor Research manufacturing partners, (in addition to the aforementioned highest ingredient testing quality standards) also meet these best practices manufacturing standards in the industry.
Each of our partners is registered with the Food and Drug Administration (FDA) and are regularly inspected by the FDA. All are in full compliance with current Good Manufacturing Practice standards (cGMP) as inspectors regularly perform full systems-based cGMP inspections at each facility. All facilities maintain current FDA acceptance letters and copies of the FDA Establishment Inspection Reports (EIR) which detail everything that FDA inspectors review.
A&Z Pharmaceutical is a leading developer, manufacturer and marketer of premium quality pharmaceutical products, and nutritional supplements, for over 25 years.
Their products encircle life, from newborns to active and aging adults, providing exceptional nutritional value and educational guidance for the well-being of the entire family. Today, A&Z Pharmaceutical operates with over 600 employees and a growing number of dedicated research laboratories and manufacturing facilities to ensure the delivery of next generation products and services to its vast customer base. Dedicated to outstanding core values, A&Z Pharmaceutical is passionate about its mission to Advance Healthier Lives® through Quality, Education, R&D, and the global service programs that allow us to embrace people worldwide.
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