13485 Certification
LSAS Labour Standards Assurance System
Training Courses
CTPAT Security Audits
Responsible Jewellery Council
UK Authorised Representative / EU Responsible person
Social Labour Convergence Program (SLCP)
SA8000 Social Accountability
Good Manufacturing Practice Certification
Signet Jewellers CoC Audits
European Down and Feather Association
Aluminium Stewardship Initiative
ISO 37001 Anti-bribery Management System (ABMS)
Worldwide Responsible Accredited Production(WRAP)
Person Responsible for Regulatory Compliance (PRRC)
MODERN SLAVERY ASSESSMENT TOOL (MSAT) HELP
MODERN SLAVERY ACT
AUTHORISED ECONOMIC OPERATOR (AEO)
INTERNATIONAL SECURITY ASSESSMENT
GLOBAL WIND ORGANIZATION
STREAMLINED ENERGY AND CARBON REPORTING (SECR)
SEDEX
IRIS
WFSGI
HIGG Index
REASONS TO CHOOSE INTERNATIONAL ASSOCIATES
International Associates provide a simple and cost effective route to certification, and are experts in the delivery of management system training and auditing.
- Fast Service
- Cost Effective
- Online Support
- Competent Personnel
- Modern & Progressive
- Understanding
- Responsive
- Professionally Managed
- International Accepted Certificates
Latest News
Medical Devices CAMD
Competent Authorities for Medical Devices CAMD explaining us the PRRC role with @Thierry Sirdey #medicaldevices #teamprrc2023 #regulatoryaffairs #eumdr
Continued recognition of UKAS
In a significant development for international accreditation post-Brexit, the Italian Council of State has upheld the validity of certifications accredited by UKAS. This decision marks a crucial juncture in maintaining…
COMMISSION DELEGATED REGULATION
The EU has just issued a new regulation relating to the UDI of contact lenses. This is a follow-up form the previous MDGC guidance. COMMISSION DELEGATED REGULATION (EU) 2023/2197 of…
Brand reputation
I’m always amazed why companies with a Brand reputation still risk the business in this way. https://www.ethicaltrade.org/blog/bbc-findings-call-question-boohoos-ethical-commitments
Certificate of Assurance
We are pleased to announce we have reconfirmed our compliance with the Cyber Essentials scheme for another year. Well done, team!
Trial Master File
What is a trial master file? If you’re a medical device manufacturer, chances are, you’ll need to conduct one or more clinical trials before you can prepare your product to…
