Cosmetic Product Safety Reports (CPSRs) play a vital role in the cosmetics industry. CPSRs are mandated by law in numerous countries worldwide, especially in the European Union (EU) and United Kingdom (UK) markets. The reports contain detailed information on ingredients and finished products, ensuring the safety of cosmetic products for consumers.
- June 6, 2023 Cosmetics Regulatory Services, Regulatory Affairs
- June 6, 2023 Cosmetics Regulatory Services, Regulatory Affairs, Regulatory Labeling
Cosmetic claims are statements made by manufacturers or marketers regarding the benefits and efficacy of their products. In the European Union (EU), cosmetic claims must comply with the strict regulations laid out in Cosmetics Regulation 1223/2009, especially Regulation 655/2013, which specifies common criteria for the justification of claims used for cosmetic products.
- June 6, 2023 Cosmetics Regulatory Services, Regulatory Affairs, Regulatory Labeling
Online cosmetic sales have become increasingly popular in recent years. With the rise of e-commerce platforms and the shift towards online shopping, it is crucial for cosmetic companies to understand the requirements for online sales so that they can ensure Regulatory compliance and provide customers with a safe and reliable shopping experience.
- June 5, 2023 Publishing & Submissions, Regulatory Software & Services
As regulatory landscapes evolve, countries worldwide are embracing the adoption of electronic Common Technical Document (eCTD) submissions to streamline their Regulatory submissions processes. One such country that will soon be venturing into the realm of eCTD submissions is Singapore.
- June 1, 2023 Cosmetics Regulatory Services, Regulatory Affairs, Regulatory Labeling
The European Union (EU) is a political and economic union of 27-member states located primarily in Europe. It represents one of the largest economic areas in the world, with a population of over 748 million people. One of the most significant challenges for businesses operating in the EU is dealing with the many different languages spoken across the region.
- June 1, 2023 Chemicals, Consumer Healthcare, Regulatory Affairs
Malaysia has established several chemical safety regulations to protect human health and the environment from potential hazards associated with the use, handling, storage, and disposal of hazardous chemicals. This blog provides an overview of the key chemical safety regulations that are currently in place in Malaysia.
Unlocking the potential of a ground-breaking pharmaceutical product requires meticulous attention to detail, especially when it comes to artwork management. In the ever-evolving landscape of regulatory compliance, where success hinges on flawless execution, there is no room for error. But why Right-First-Time Artwork?
- May 30, 2023 Medical Devices
Reprocessing refers to the method through which you can reuse medical devices safely and effectively.
- May 30, 2023 Medical Devices
The European Union Medical Device Regulation (EU MDR) has replaced the Medical Device Directive (MDD) and the Active Implantable Medical Device Directives (AIMDD), introducing several significant changes in the regulations. One of the key elements that has been replaced is Essential Requirements (ER). ER have now been replaced by General Safety and Performance Requirements (GSPR).
- May 26, 2023 Pharmacovigilance, Pharmaceuticals, Regulatory Affairs
The COVID-19 pandemic has brought about unprecedented changes in the healthcare industry, including the Pharmacovigilance (PV) process. The pandemic re-emphasized the role of PV in the pharmaceutical industry. As personalized medicine gained popularity, the tactics of pharmaceutical manufacturers and the PV process flow for ensuring the end-user’s safety had to alter.