AXIOM COMPLIANCE GROUPMarket access starts with identifying applicable requirements. We review product use, characteristics and destination markets, help prepare documentation and coordinate the required procedures with independent organizations.
We review the product name, model, manufacturer, intended use and technical parameters. We check supply documents and identify the assessment route, testing and supporting documentation.
We review product characteristics, manufacturing processes and quality control. We help organize standards, technical documents and information for the selected assessment procedure.
We coordinate preparation and interaction with an independent certification body. Implementation, internal auditing and training are covered in the relevant service section. Certification follows the applicable independent assessment procedure.
HALAL, organic certification, OEKO-TEX® STANDARD 100, CE, EAC, RoHS and FDA. Requirements are selected for the product and market. FSSC 22000, GLOBALG.A.P. and GMP+ are considered according to the business activity.
Initial review, requirements list, work plan, document preparation and coordination of testing and project participants. If nonconformities are found, we discuss the required corrective actions.
Product name, model, manufacturer, country of manufacture, use, specifications, photographs, documents and target market. Further information may be requested. Scope, schedule and pricing are agreed after review.
What is it? Preparation for demonstrating product conformity with applicable requirements of the selected market.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? Requirements of the selected scheme for raw materials, ingredients, production, storage and traceability, taking account of the market.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? Organic production rules of the selected market: permitted inputs, separation of flows, suppliers and traceability. A conversion period may be required.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? Testing textile products and components for harmful substances; requirements depend on the product’s use category.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? Marking for products covered by relevant EU legislation. We review applicable requirements, the technical file, testing and declaration, and notified body involvement where required.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? A conformity mark following the required assessment under applicable EAEU technical regulations. The assessment form depends on the product.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? Restriction of certain hazardous substances in applicable electrical and electronic equipment. We review components, materials and supporting evidence.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
What is it? US requirements for the regulated product category. We review registration, listing and other procedures, including market authorization for certain medical devices. Registration alone is not FDA approval.
AXIOM COMPLIANCE GROUP support. We clarify scope and requirements, review initial data and agree documents and procedures. We coordinate preparation and interaction with competent independent participants.
Tell us about your product, company or project and we will discuss the requirements and the necessary steps.
Phone
+998 99 885 90 10
Email
info@axiomgroup.uzstandart.tashkent@mail.ru
Address
100043, Toshkent shahri, Chilonzor tumani, Zarkand 1-berk ko‘chasi, 11-uy
Tashkent, Chilanzar district, Zarkand 1st dead end, building 11