The Health Sciences Authority (HSA), Singapore regulates the sale and import of cosmetics in the country. All cosmetics that are intended for sale in Singapore must be notified to the HSA before they are sold. The Regulatory process of the HSA involves the submission, notification, and re-notification of cosmetic products. This blog will tell you all you need to know about the current regulations.
- July 14, 2023 Cosmetics Regulatory Services, Regulatory Affairs, Regulatory Labeling
Introduction
Launching cosmetics in Nigeria can be a promising venture due to the large consumer base for cosmetic products in the country. However, navigating the Regulatory landscape can present significant challenges. In this blog, we will explore the key Regulatory hurdles that businesses face when launching cosmetics in Nigeria.
- July 13, 2023 Regulatory Affairs, Publishing & Submissions
Introduction
Regulatory submissions of clinical and non-clinical datasets play a vital role in the approval process of pharmaceutical products. These submissions provide Regulatory authorities with crucial evidence of the safety, efficacy, and quality of the products.
- July 13, 2023 Regulatory Affairs, Publishing & Submissions
Regulatory compliance is an essential aspect of the Healthcare and Pharmaceutical industries. One crucial aspect of compliance is the submission of various applications to Regulatory authorities. In the United States, the United States Food and Drug Administration (US FDA) plays a significant role in ensuring the safety and efficacy of drugs, medical devices, and biologics.
- July 13, 2023 Regulatory Affairs, Regulatory Labeling
Combination products, or products that combine medicines, devices, or biologics pose special Regulatory labeling problems. As these products consist of multiple components and varying Regulatory standards, manufacturers must ensure that they comply with all the individual requirements and properly convey safety information.
- July 11, 2023 Pharmaceuticals, Regulatory Artwork Services, Regulatory Affairs
In the global pharmaceutical industry, accurate and error-free communication is of paramount importance. As pharmaceutical companies expand their reach into international markets, multilingual materials such as product labels, packaging, and patient information leaflets are required more and more.
- July 11, 2023 Food and Food Supplements, Regulatory Affairs
Introduction
Natural Health Products (NHPs) have gained significant popularity among consumers in Canada. However, manufacturers and distributors must comply with the Regulatory requirements set forth by Health Canada (HC) before launching and selling NHPs in the Canadian market. In this blog, we shall explore the process of launching and registering NHPs in Canada, outlining the essential steps involved.
- July 10, 2023 Pharmaceuticals, Regulatory Affairs
Agência Nacional de Vigilância Sanitária (ANVISA), or the Brazilian Health Regulatory Agency/National Health Surveillance Agency, approved Apretude® (cabotegravir), in both tablet and injectable dosage forms, on June 05, 2023, for the prevention of Human Immunodeficiency Virus (HIV) viral transmission.
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
The global Vitamin D supplement market is projected to grow at a CAGR of 7.34% during the forecast period (2022–2027). It is segmented into two (02) product types:
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
In the food and dietary supplements industry, maintaining the highest standards of quality and safety is of paramount importance. This is where Good Manufacturing Practices (GMP) requirements come into play. GMP provides manufacturers with a framework of strict guidelines and protocols, ensuring the integrity of their products.