Our plants maintain documentation related to the entire manufacturing process (including stability tests), and we offer our clients full traceability for all products and at every stage, including intake, storage, sampling, testing, qualifying or disqualifying of raw or packaging materials, production, packaging, release or disqualification of formulas, shipping, and more.
Our strict quality assurance process ensures full precise and detailed documentation of all laboratory procedures for future reference. As a result, the solutions are sampled for stability on a continuous basis, and kept under controlled conditions for a period of 7 years.
We operate under strict GMP regulations and adhere to globally recognized standards in addition to our rigorous internal quality control practices. We are ISO Certified for 9001, 13485, and 22716 standards, and operate our facility in strict adherence to both the Israeli Ministry of Health and Ministry of Environment’s requirements.
We are also proud to adhere to FDA and Colipa protocols for all products destined for the US and EU markets respectively, and carry the Ecocert Certificate for our range of Natural Products. In addition we follow highest environmental standards, and do not perform any experiments on animals.
Having grown out of the highly regulated pharmaceutical industry, we pride ourselves on having a highly advanced regulatory department. Liaising with our customers worldwide, our team ensures that all products meet and exceed regulatory standards, including assisting with all necessary filings and submissions related to the introduction of new products to each geographic market.
As standard practice we remain up to date with current and emerging legislation, and ensure with all product documentation is kept in order as it relates to registrations and notifications, raw ingredient clearance, labeling, claim substantiation and complaint monitoring.