Requirements for cosmetic products on eu market, cosmetics compliance process eu market, obligations for cosmetics manufacturers Europe
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New guidelines on clinical evidence, clinical investigation and clinical evaluation
What do the New Guidelines from the International Medical Device Regulators Forum include? Read on the clinical evidence, clinical investigation and clinical evaluation.
Several important opinions issued by the SCCS
The Scientific Committee on Consumer Safety (SCCS) recently scrutinized several ingredients, commonly used in various cosmetics products.
National authorities start fining for GDPR breaches
GDPR infringement, GDPR fines, data protection rules
Why is label review one of the last steps in the compliance process?
Answering questions on the cosmetics products labelling process. When should you label your product? Find out with Obelis' EU regulatory consulting team.
Is the Irish health sector prepared for an eventual Brexit?
Companies are requested to ensure sufficient stock and continuity of supply during the transition. Start your compliance roadmap with Obelis.
Spain is ready for Brexit: new checklist for Medical Devices and Cosmetics
The Spanish Agency of Medicines and Medical Devices (AEMPS) has published a Checklist to verify the Brexit readiness of companies based in Spain in the sectors…
New EU Regulation on Market Surveillance and Compliance of Products
The new Regulation sets out an obligation for economic operators to cooperate with the market surveillance authorities and establishes a framework for the control of products entering the Union market.
MDR Transitional regime clarified by MDCG
The Medical Devices Coordination Group (MDCG) has published a document on the validity of certificates issued in accordance to the Directive after the new Medical Device Regulation (MDR) becomes applicable.
OEM with European ambition?
Having a commercial brand is not necessary, even as an OEM you can register your products in the CPNP and enjoy the benefits.