Trust Dor Pharmaceutical Services to smoothly navigate the regulatory landscape, which is stricter than other countries, such as the US.

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Regulatory Affairs

Regulatory affairs department outsourcing New product submissions and follow-up till approval Post-approval support (renewals, variations, import issue resolution, extensions for additional claims, etc.) Business development and due diligence Regulatory affairs consulting Regulatory second opinions.

Cosmetics Labeling & Localization

In Israel’s stringent regulatory environment, Dor’s cosmetics labeling, packaging and localization solution offers outstanding advantages for quality, speed and compliance. Dor adapts and translates all labeling elements to local regulatory requirements, formats and languages, designs graphic artwork and prints all cosmetics packaging elements so they are ready for assembly.

Preparation of labeling and packaging

Preparation of labeling and packaging materials for cosmetics under Good Manufacturing Practice (GMP) standards including translation and graphics.

Laboratory testing

Laboratory testing and clinical trials according to registration requirements to meet requested claims

Writing, assembling & maintenance

Writing, assembling & maintenance of the Cosmetic Product Information File (PIF) your products as required under the new directive