In our pursuit of revolutionary treatments, we challenge medical methodologies and explore new possibilities to develop drugs and supplements, intervene earlier in chronic illnesses, and find ways to drastically improve quality of life.
At Pacific Vital we take pride in our advanced labs and in our researchers who work tirelessly to develop unique pharmaceutical products to meet the needs of consumers. We based our research on enhancing what exists in the market to develop the next generation of medications and supplements. With consumers’ needs in mind and for the betterment of the health of society our scientists spend years formulating this next generation of medications and supplements meanwhile focusing on the quality of the raw materials. Our medications and supplements target different aspects of each health issue they are designed for without losing sight of side effects and overall human health. We are proud to announce we have several products in our pipeline in phases two and three of production getting completed to be manufactured soon.
Our pipeline information may include a reference to an investigation agent, or an investigational use of the FDA approved product. Safety and efficacy for investigational uses or agents have not been established or approved by the FDA. This table provides an overview of selected projects in development and can be filtered by both therapeutic area and development phase.
We are relentlessly pursuing the innovations of tomorrow with our broad and diverse pipeline of potential first or best-in-class investigational medicines designed to treat a range of diseases across our focus areas of neurology, cardiology and select areas of high patient needs.
Our portfolio is based on novel scientific targets with the potential for therapeutic application across multiple liver diseases, with a focus on those with high unmet need.
We are leveraging our decades of research and background in bile acids and FXR agonism to expand our pipeline to deliver effective treatments for the growing number of people living with chronic liver diseases.
At the start of any new drug development is an understanding of a disease, the discovery of a medication and a choice of the most active substances to provide relief or prevention. It takes two to three years for medication to be created.
The compound, also called investigational product, is compared either to a placebo (a substance with no pharmacological activity) or to existing treatments, to decide if it is more or less effective. The clinical trial determines the effective dose, possible toxicity and the nature and frequency of undesirable side effects.
Pacific Vital Inc. supports a wide range of partners worldwide, particularly in the dietary supplement, personal care, and pharmaceutical industries. Many people take various forms of dietary supplements to boost health and well-being or address deficiency symptoms. For nutritional supplements to achieve their desired effect, their composition and exact dosage of the active ingredient is essential.
As an experienced player with dedicated labs in nutritional supplement testing, we not only determine the exact composition of your product’s active ingredients but further test them for possible unwanted residues or contaminants. Also, we can provide you with qualified and dependable advice regarding the production of your nutritional supplements.
The stability and integrity of your products over time are crucial to your product brand. Our Company offers both Real-Time and Accelerated Stability and Shelf-Life studies to provide you with data to support your best by or expiration dates.
Contact our Samples Management Team or Partnerships Team for more information and a detailed quote on services, pricing, and testing intervals.
Simply provide us with a copy of your product label, and together we will explore your options. We will help you every step of the way.
Analytical testing results are only as good as the equipment and methods used. Highly trained scientists dedicated to quality and accuracy, using validated methods, are essential to our success. Pacific vital’s strict adherence to Good Laboratory Practices, ISO Accreditations, and robust quality training of our team members are the keys to generating accurate and reliable results. We employ state-of-the-art analytical equipment such as HPLC, GC, GC-MS, ICP-MS, PCR, and more, all under preventative maintenance schedules, which help us maintain consistent and reliable turnaround times and accuracy.
After researching a compound, labs test it in vitro and then on animals. These steps evaluate the compound’s effectiveness and tolerance. If all the data is satisfactory, the next step is to consider tests on humans. The pharmaceutical manufacturer then submits a request to an Independent Ethics Committee (IEC) or Institutional Review Board (IRB), a completely independent organization whose job is to monitor the test procedures. Once the committee approval is obtained, the clinical trial will proceed but the participants’ safety has to be kept in mind throughout the process.