Overview
Complete guidance on CE marking requirements for products destined for EU markets — covering applicable directives, testing, and declaration of conformity.
Who This Is For
Exporters targeting EU markets with regulated product categories.
Estimated Timeline
What This Includes
- Applicable directive identification
- Technical file preparation guidance
- Testing laboratory identification
- Declaration of Conformity template
- CE marking application
What You Receive
CE marking roadmap
Technical file guide
Testing lab referrals
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Overview
Guidance on FDA registration for food, cosmetics, medical devices, and dietary supplements destined for the US market.
Who This Is For
Food, cosmetic, and medical device exporters targeting the US market.
Estimated Timeline
What This Includes
- FDA product category assessment
- Registration process guidance
- US Agent identification
- Labelling compliance review
- Prior notice coordination
What You Receive
FDA registration roadmap
US Agent contacts
Labelling compliance guide
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Overview
Coordination of ISO certification processes (ISO 9001, 14001, 22000, etc.) — from gap assessment to certification body selection and audit preparation.
Who This Is For
Manufacturers and exporters seeking to gain buyer trust through ISO certification.
Estimated Timeline
What This Includes
- Relevant ISO standard identification
- Gap assessment
- Certification body selection
- Documentation preparation
- Pre-audit preparation
What You Receive
ISO readiness report
Certification body shortlist
Pre-audit checklist
Ready to start?
Get expert guidance tailored to your business needs.