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Does CLP Regulations apply to Cosmetic Products?
Advena Cosmetic Responsible Persons Service Cosmetic News – 2025
Advena recognised as Medical Device Regulatory Consulting Company of the Year
Meet With Us… ADVENA LTD UK ARE EXHIBITING AT ARAB HEALTH 2025 – 27th to 30th January
Advena Celebrates as Patron of The Commonwealth at 75 – Watch the Highlights from Westminster Abbey
Reporting interruption or discontinuation of the supply of medical devices – EU 2024/1860
PSUR Guidance for Medical Device Manufacturer
Significance of the SOTA section in the CER
Are QR Codes the future of the Cosmetic Labelling?
Urgent Reminder on the Amendment to Labelling of Fragrance Allergens in Cosmetic Products
Announcement Update on Labelling for UK EPR
Advena announces the promotion of James Bradbury to Operations and Compliance Director
Advena Announced as Patron of The Commonwealth at 75
Who should I choose for ISO13485 certification – a Certification or Notified Body?
Navigating UDI – Highlights from Webinar hosted by GS1
Introducing Nirjit Nahal: Our New Quality Systems Specialist
Are YOU ready for the next EU MDR deadline?
The new Regulation (EU) 2024/1860, amending Regulations (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR). What do manufacturers need to do?
EN ISO 10993 – Biological Evaluation of Medical Devices – Q&A’s
Outsourcing Person Responsible for Regulatory Compliance (PRRC) Article 15 EU MDR 2017/745 or IVDR 2017/746
Mastering Clinical Evaluation Through Equivalence: What are the opportunities and pitfalls?
What Essential Clinical Evidence Is Needed for Legacy Devices?
Top 5 audit non-conformities raised by BSI
A dedication to Alison Harris
Are you ready for 26th May 2024 deadline?
Do you have a Class I device that will be up-classified under MDR EU 2017/745?
The Legal Impacts of Non-Compliance – How to prevent a manageable issue from escalating into a crisis
eQMS Software – Getting it right first time
Regulatory Compliance
How Compliance Affects Your Business and Legal Defense
Bespoke Medical Device Training Services by Advena Consultancy
Simplify Medical Device Regulation with Advena Consultancy
Streamlining Device Regulatory Compliance for SMEs
Hybrid Audits
MHRA yellow card
Audits – Preparing For The Year To Come
Contact Us
+44 1926 800 153
Home
Services
Medical Device Consultancy
In-Vitro Diagnostic Consultancy
UK Responsible Person
Person Responsible for Regulatory Compliance (PRRC) Services
Quality Management
Medical Device Single Audit Program
Mentoring Service
Auditing Services
Training Services
Cosmetics UK & EU Responsible Person Services
Activ QMS Software
Quality Management System Modules
Example Packages Available
Book a Demonstration
Testimonials
Contact Us
Meet the Team
About Us
News
Does CLP Regulations apply to Cosmetic Products?
Advena Cosmetic Responsible Persons Service Cosmetic News – 2025
Advena recognised as Medical Device Regulatory Consulting Company of the Year
Meet With Us… ADVENA LTD UK ARE EXHIBITING AT ARAB HEALTH 2025 – 27th to 30th January
Advena Celebrates as Patron of The Commonwealth at 75 – Watch the Highlights from Westminster Abbey
Reporting interruption or discontinuation of the supply of medical devices – EU 2024/1860
PSUR Guidance for Medical Device Manufacturer
Significance of the SOTA section in the CER
Are QR Codes the future of the Cosmetic Labelling?
Urgent Reminder on the Amendment to Labelling of Fragrance Allergens in Cosmetic Products
Announcement Update on Labelling for UK EPR
Advena announces the promotion of James Bradbury to Operations and Compliance Director
Advena Announced as Patron of The Commonwealth at 75
Who should I choose for ISO13485 certification – a Certification or Notified Body?
Navigating UDI – Highlights from Webinar hosted by GS1
Introducing Nirjit Nahal: Our New Quality Systems Specialist
Are YOU ready for the next EU MDR deadline?
The new Regulation (EU) 2024/1860, amending Regulations (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR). What do manufacturers need to do?
EN ISO 10993 – Biological Evaluation of Medical Devices – Q&A’s
Outsourcing Person Responsible for Regulatory Compliance (PRRC) Article 15 EU MDR 2017/745 or IVDR 2017/746
Mastering Clinical Evaluation Through Equivalence: What are the opportunities and pitfalls?
What Essential Clinical Evidence Is Needed for Legacy Devices?
Top 5 audit non-conformities raised by BSI
A dedication to Alison Harris
Are you ready for 26th May 2024 deadline?
Do you have a Class I device that will be up-classified under MDR EU 2017/745?
The Legal Impacts of Non-Compliance – How to prevent a manageable issue from escalating into a crisis
eQMS Software – Getting it right first time
Regulatory Compliance
How Compliance Affects Your Business and Legal Defense
Bespoke Medical Device Training Services by Advena Consultancy
Simplify Medical Device Regulation with Advena Consultancy
Streamlining Device Regulatory Compliance for SMEs
Hybrid Audits
MHRA yellow card
Audits – Preparing For The Year To Come
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