For medical device companies looking to enter the Canadian market, understanding and complying with regulatory requirements is essential. Health Canada has introduced new regulations, including the Medical Device Single Audit Program (MDSAP), to streamline the process for both manufacturers and regulators.
This workshop is beneficial for professionals involved in regulatory affairs, quality assurance, product development, manufacturing, and clinical development. Gain valuable insights into Canadian regulatory requirements, risk management, quality systems, and more. |
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