Techlink International
Regulatory consultancy and compliance service provider specializing in labeling, testing coordination, and certification for products entering Mexico, Canada, and the U.S. Offers end-to-end in-house services including label design, Spanish localization, project management, test coordination with accredited laboratories and certification bodies, and regulatory representation for medical devices (U.S.).
Industries
N/A
Nr. of Employees
small (1-50)
Services
End-to-end labeling compliance for Mexican NOMs including label adaptation, Spanish localization, regulatory review, and issuing of Constancia documentation.
Coordination of laboratory testing and certification processes for NOM standards (safety, energy, sanitary, RF) with accredited labs and certifiers.
Adaptation of existing artwork to meet regulatory formats or provision of compliance stickers when full packaging redesign is impractical.
Designation as a U.S. Agent and/or initial importer for foreign medical device and IVD manufacturers to liaise with FDA and support registration/listing and inspection coordination.
CFIA-focused services including regulatory review, formula review, bilingual label development, verification, and regulator support for Canadian market entry.
Technical and regulatory guidance for short-range radiocommunication devices to meet frequency, power, stability, and labeling requirements under NOM-208 and IFT provisions.
End-to-end labeling compliance for Mexican NOMs including label adaptation, Spanish localization, regulatory review, and issuing of Constancia documentation.
Coordination of laboratory testing and certification processes for NOM standards (safety, energy, sanitary, RF) with accredited labs and certifiers.
Adaptation of existing artwork to meet regulatory formats or provision of compliance stickers when full packaging redesign is impractical.
Designation as a U.S. Agent and/or initial importer for foreign medical device and IVD manufacturers to liaise with FDA and support registration/listing and inspection coordination.
CFIA-focused services including regulatory review, formula review, bilingual label development, verification, and regulator support for Canadian market entry.
Technical and regulatory guidance for short-range radiocommunication devices to meet frequency, power, stability, and labeling requirements under NOM-208 and IFT provisions.
Expertise Areas
- NOM compliance and certification (Mexico)
- Labeling compliance for food, cosmetics, textiles, electronics, and household products
- Regulatory consulting for product classification and claims
- Testing coordination with accredited laboratories
Key Technologies
- RF compliance testing (band occupancy, output power, frequency stability)
- Microbiological testing for sanitary compliance
- Chemical contaminant analysis (heavy metals, pesticide residues)
- Nutrition panel calculation and front-of-package warning assessment
News & Updates
Overview of laboratory testing and certification processes necessary for commercialization in the Mexican market and how NOM standards govern testing requirements.
Discussion of the institutional transition affecting telecommunications regulation and implications for device homologation and spectrum management in Mexico.
Explanation of NOM-186 certification requirements for cocoa and chocolate products including sanitary and compositional testing and label verification.
Overview of requirements and regulatory considerations for bringing medical devices to the Canadian market and the role of regulatory consulting.
Discussion of Mexico's regulatory framework for product labeling and practical considerations for exporters entering the Mexican marketplace.
Summary of the mandatory health and commercial information required on labels for chemical coatings and related products under the NOM-003 standard.
Overview of laboratory testing and certification processes necessary for commercialization in the Mexican market and how NOM standards govern testing requirements.
Discussion of the institutional transition affecting telecommunications regulation and implications for device homologation and spectrum management in Mexico.
Explanation of NOM-186 certification requirements for cocoa and chocolate products including sanitary and compositional testing and label verification.
Overview of requirements and regulatory considerations for bringing medical devices to the Canadian market and the role of regulatory consulting.
Discussion of Mexico's regulatory framework for product labeling and practical considerations for exporters entering the Mexican marketplace.
Summary of the mandatory health and commercial information required on labels for chemical coatings and related products under the NOM-003 standard.