Industry & Innovators
Scientific studies
IPAR's scientific studies are based on our expert research spanning more than 20 years, including anti-aging, immunity system, and women's intimate hygiene. We are an innovational company with products dependent on scientific studies and critical learnings. We do not rely on testimonials for evidence.
TALK WITH SCIENCE
At IPAR, our product innovation begins with scientific insights backed by a quality process that we call ISPC methods* (IPAR Statistical Process Control methods). Our scientists’ range of scientific disciplines allows us to foster limitless new avenues of inquiry and innovation
We are inspired by innovative and technologies; We are willing to with our sustainable technical solution to help people's live quality lives.
ISPC Methods
ISPC methods were inspired by the DMAIC project. Its methodology involves defining the system, the voice of the customer, and the project goals. We then measure key aspects of the current process and collect relevant data, then analyse the data to investigate and verify cause-and-effect relationships.
CENTRAL LAB
The Center Lab is involved in all aspects of the selection, safety, and substantiation phases. The labs are used for the development and evaluation of IPAR products.
Central Lab is where new ingredients and active components are discovered and also where analytical methods for new ingredients and finished products are developed. Here, scientists research and develop natural extracts and new products, coordinate studies with them, and determine levels of active ingredients and purity to ensure product integrity and proper ingredient selection.
Plant-based Capsules Designed
Ipar is go-to resource for capsule manufacturing. With ethically sourced, premium-grade ingredients and an unwavering commitment to exceptional service, we will work with every step of the way to develop every formulation
MANUFACTURING
IPAR's manufacturing facility has established high-quality control mechanisms and a quality-assurance system; the facility passed the third-party regulatory authorities.