Regulatory affairs manager

Cannara Biotech (Québec) inc

Farnham, QC

General Summary
• Manage licensing and communications with Health Canada;
• Provide regulatory requirements expertise to other departments during
product development or proposed product changes
approved (including R&D, manufacturing, quality assurance, quality control and
marketing);
• Research and analyze regulatory information and determine acceptability of
product data, procedures and other documentation submitted in support of
Product registration;
• Prepare, review, analyze and consolidate all information required for
initial or post-approval regulatory submissions to competent authorities, y
including Health Canada;
• Write related technical parts of the detailed summaries that are included in the
submission filed with regulatory authorities;
• Ensure compliance with government regulations by providing agencies
all necessary information relating to the changes or
changes to the company’s products;
• Review technical and clinical literature and recommend changes
in labelling... More Detail

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