EU Responsible Person Offices:
Belgium, Marcel Broodthaer square 8
Brussels, 1060
Phone: +32(0)2-892-3964
Italy, via San Senatore 14
Milano 20122
Phone: +39 3405180274
United Kingdom, Hamilton House
Mabledon Place, London
WC1H 9BB
Angel Consulting London Ltd
7 Lanark Square UK-London E14 9RE
News: read all the EU regulations and guidelines updates online for free
About Us
History
Angel Consulting was born as an evolution from a single consultant’s work with the idea for supporting cosmetic companies. The project was born in the year 2000 and now it’s a developed company with a highly qualified team focused on clients’ most critical issues and opportunities.
Goals
We want to help you to achieve your goals successfully.
We seek to improve your effectiveness in the global market, giving our full attention to the compliance of your products.
We guarantee success in reaching your full potential.
Values
We believe that we can help you develop your projects in the best way possible supporting you with our main qualities like discretion, ethic, collaboration and problem-solving skills
Vision
Since the beginning, Matteo Zanotti Russo’s vision has been based on providing you with both high skill and direct contact. An eye on cosmetic counseling, safety assessment, import-export, but always focused on a direct relationship with a qualified person always supported by a knowledgeable team and more.
Cosmetics Legislation in EU
Regulation (EC) 1223/2009
The Regulation (EC) 1223/2009 that replaces the Directive 76/768/EC with all amendments, implements and clarifies some of the obstacles and trouble points that were present in the past legislation.
The regulation, in force since 11 July 2013, focuses its attention on some keywords revised and redefined: in particular, the appointment of the Responsible Person, the implementation of the product information file (PIF), and the application of the good manufacturing practice according to ISO 22716:2007:
Medical Device Legislation in EU and UK – EU 2017/745-6
UK Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002)
EU: 2017/745 and 746 for Medical Devices and In Vitro Diagnostics:
MD in UK after Brexit:
Responsible person
The Responsible Person (RP) is a “legal” or “natural” person designated within the European Union who will assume technical and legal responsibilities as the unique representative throughout the EU.
Product information file (PIF)
PIF is a collection of documents that describe a cosmetic product. It includes a Safety Assessment signed by a qualified expert.
Good Manufacturing Practice GMP
ISO 22716:2007 is the international standard that gives guidelines for cosmetic production, control, storage, and shipment in compliance with Regulation (EU) No. 1223/2009.
Import & Export
Import assistance in EU, Export assistance, Labelling & Packaging, and Technical assistance. Angel Consulting is a successful expression of high-tech/multi-skills service for your business.
Cosmetics. Advice. Surveillance.
Our Project
