Peru’s Food and Nutrition Security Law, also known as Law No. 31315, marks a significant legislative milestone aimed at bolstering food security and nutritional well-being across the country. This law encompasses various facets of food safety, access to nutritious food, and public health.
- April 10, 2024 Food and Food Supplements
- April 10, 2024 Food and Food Supplements
Saudi Arabia, along with several other countries in the region, has taken a significant step toward bolstering food safety and protecting consumer health through the introduction of a draft technical regulation on requirements of nutritional labeling.
- April 10, 2024 Food and Food Supplements
Launching Food for Special Medical Purposes (FSMP) in China requires a profound understanding of the Regulatory landscape of the food and dietary supplement market. Governed by the State Administration for Market Regulation (SAMR), the FSMP rules are carefully designed to safeguard the safety, quality, and efficacy of specialized food products tailored for individuals with specific medical conditions.
- April 4, 2024 Pharmaceuticals, Regulatory Artwork Services
Advanced Therapy Medicinal Products (ATMPs) represent a cutting-edge approach to medicine, harnessing the power of cells, tissues, or genes to treat a variety of ailments. Due to their complexity and novelty, regulatory requirements for Advanced Therapy Medicinal Products (ATMPs) are understandably stringent.
- April 3, 2024 Cosmetics Regulatory Services, Regulatory Affairs
The cosmetic market in Thailand is a thriving one, offering a diverse range of beauty and personal care products. The country has established a comprehensive Regulatory framework to ensure consumer safety and uphold product quality. Thus, manufacturers, importers, and consumers must understand the cosmetic Regulatory scenario in Thailand before launching their products.
- April 3, 2024 Cosmetics Regulatory Services, Regulatory Affairs
The cosmetic market in Vietnam is a flourishing one, offering a diverse range of beauty and personal care products. The country has established a comprehensive Regulatory framework to ensure consumer safety and uphold product quality. Thus, manufacturers, importers, and consumers must understand the cosmetic Regulatory scenario in Vietnam before setting forth to launch their products.
- March 29, 2024 Medical Devices, Regulatory Affairs
Post the Brexit scenario, the Regulatory landscape for medical devices in the United Kingdom (UK) underwent a profound metamorphosis, significantly impacting manufacturers aiming to introduce their products. As the UK made an exit from the European Union (EU), there was a shift from Conformité Européenne (CE) marking to UK Conformity Assessed (UKCA) marking.
- March 29, 2024 Medical Devices, Regulatory Affairs
The current Regulatory scenario for medical devices in the United Kingdom (UK) is governed by the Medical Devices Regulations 2002 (SI 2002 No. 618, as amended), also known as the UK MDR 2002.
- March 29, 2024 Medical Devices, Regulatory Affairs
The specifics for medical devices refer to a set of technical and/or clinical requirements, other than a standard, that provides a means of complying with the legal obligations applicable to a device, process, or system. This includes the type of medical conditions the device is designed to diagnose, treat, monitor, alleviate, or prevent.
- March 29, 2024 Medical Devices, Regulatory Affairs
In the ever-evolving healthcare landscape, personalized medical devices have emerged as a groundbreaking approach, tailoring treatments to individual patients based on their unique characteristics. These include devices that are custom-made or personalized to be adaptable to the patients’ solutions.