Global Market Access

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Global Market Access

Global Market Access

Region-wise certifications for smooth international entry.

Entering international markets requires more than just exporting your products —it demands compliance with country-specific regulations, product certifications, and safety standards.

At Markek International Certifications, we facilitate Global Market Access (GMA) by helping businesses navigate regulatory requirements, obtain mandatory certifications, and ensure seamless market entry into regions like Saudi Arabia, GCC, India, Europe, and the USA.

Why Global Market Access Matters?

Navigating trade regulations can be challenging. Each country enforces specific laws for product safety, labeling, certification, and documentation. Non-compliance can result in:

By partnering with Markek International Certifications, businesses can ensure:

Steps to Achieve Global Market Access

Identify Regulatory Requirements

Understand the technical regulations and conformity procedures for the target country or region.

Obtain Product Certification

Secure approvals under relevant schemes like SASO, BIS, G-Mark, CE, FCC, or other market-specific frameworks

Identify Regulatory Requirements

Ensure testing and inspection are carried out by accredited labs and bodies in line with required standards.

Prepare Labeling & Documentation

Verify packaging, labeling, user manuals, and technical files meet destination market requirements.

Evaluate Risk & Compliance

Address compliance gaps and assess any risks related to product safety, rejection, or delays.

Maintain Ongoing Certification

Understand the technical regulations and conformity procedures for the target country or region.

Achieving compliance for global market access involves a structured understanding of each country’s regulatory landscape. The process typically begins with identifying the applicable technical regulations, standards, and conformity assessment procedures based on the product type and target market. Products must undergo testing in accredited laboratories to verify compliance with the relevant national or international standards. Comprehensive technical documentation is then prepared, including test reports, declarations of conformity, and labeling information, as required by regulatory authorities.

In certain jurisdictions, manufacturers without a local presence may be required to appoint an authorized representative to act on their behalf during the certification process. Post-submission interactions with certification bodies or authorities may involve responding to technical queries, updating documentation, or clarifying product specifications. Additionally, internal teams may need training on technical standards to ensure proper implementation of compliance measures across the product lifecycle. Ongoing monitoring of regulatory updates is also essential to maintain compliance as standards and market requirements evolve

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