• Home
  • Global Regulatory Affairs Services
    • Introduction
    • Pharmaceutical
      • Requirements of Health Authorities
      • Drug Application Process
      • Meeting with Health Authorities
      • Electronic Common Technical Document (eCTD)
      • Register of Innovative Drugs
      • Submissions Comparing to Innovative Drugs
      • Product Monograph
      • Drug Label Compliance
      • Filing of Information and Material to Health Authorities
      • Evaluation of Submissions
      • Pharmacovigilance
    • Natural Health Products
      • NHP Documentation Review
      • NHP Product Registration Submissions
      • Natural Health Product Site Licence
    • Medical Device
      • Medical Devices Services
      • Medical Device Application Process
      • Medical Device class II, III and IV
  • Market Expansion Services
  • Contact Us
Atinza Canada Inc.Atinza Canada Inc.
  • Home
  • Global Regulatory Affairs Services
    • Introduction
    • Pharmaceutical
      • Requirements of Health Authorities
      • Drug Application Process
      • Meeting with Health Authorities
      • Electronic Common Technical Document (eCTD)
      • Register of Innovative Drugs
      • Submissions Comparing to Innovative Drugs
      • Product Monograph
      • Drug Label Compliance
      • Filing of Information and Material to Health Authorities
      • Evaluation of Submissions
      • Pharmacovigilance
    • Natural Health Products
      • NHP Documentation Review
      • NHP Product Registration Submissions
      • Natural Health Product Site Licence
    • Medical Device
      • Medical Devices Services
      • Medical Device Application Process
      • Medical Device class II, III and IV
  • Market Expansion Services
  • Contact Us

ATINZA CANADA INC. Global Expertise in Regulatory Affairs Get the growth you need to succeed Market Expansion Services RESPONSIBLE & RELIABLE We value our prestige with customers Caption Text4 We stand by our commitment Better - Faster - Easier No compromise over Quality Passion for excellence

Global Regulatory Affairs Services

  • Provides regulatory assessment, strategy, and guidance for the clients to customize to theirs unique needs and budgets
  • Work closely with clients to ensure label of pharmaceutical products will comply strictly with the labeling requirements
  • Provide ongoing submission expertise to achieve regulatory approval
    Advise clients relating requirements in other relevant regulatory guidelines, policies and technical documents.

Market Expansion Services

  • Coordinating market research
  • Planning, developing and organizing marketing activities to support sales objectives
  • Create promotional strategies and campaigns to reach target sale quantities.
  • Advising on selection of products, pricing, advertising and sales promotion, selling, and distribution channels according to market demands.

Trading partner

  • Provide sourcing solution for customers for all products they need. We find trust worthy partners/manufacturers will can provide long term flow of products and ensure shipment are handled timely and smoothly.
  • Ensure strict supply standards and only establish business relationship with  ethical suppliers. Our commitment is to assure win-win for both customers and suppliers and mutual and sustainable development for both parties.

Contact Us

Please let us know if you have any inquiries.

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