Resources

On 10 November 2021, The UK’s Department of Health and Social Care published its guidance regarding trademark and brand names which co…

As of 1st January 2022, the Eurasian Economic Union (EAEU), formed by Belarus, Kazakhstan, Russia, Armenia, and Kyrgyzstan, will enforce the…

The Medical Devices Coordination Group (MDCG) which is the expert panel of the EU Member States and the EU Commission published on 20 Octobe…

These new requirements list what is required when Nucleic Acid is used as a raw material in health foods and supplements. The announcement s…

The Japanese Pharmaceutical and Medical Devices Law (PMDL), which is the law that regulates cosmetic products and cosmetic quasi-drugs in Ja…

EU members states have approved the EU Commission’s proposal to ban E171- Titanium Dioxide, as a food additive following a meeting of …

In order to provide a clear regulatory framework at a national level for products made only with ingredients of plant origin, vegan/vegetari…

The draft Regulation is a revised version based on a previous version which was published in 2016, it applies to all Food for Special Medica…

In October 2021, SFDA published on the Istitlaa platform a new draft technical regulations for ‘food supplements’ for public and…

On 21st Oct, China National Center for Food Safety Risk Assessment issued several food additives and nutrition fortifier approval. The new a…