
Staying Ahead of the Game: Key Insights on the Latest Requirements for New Drug Submissions
From FDA guidelines to global regulatory standards, understanding the nuances of each requirement is essential to ensure a timely
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From FDA guidelines to global regulatory standards, understanding the nuances of each requirement is essential to ensure a timely
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The healthcare industry is constantly evolving, and with the introduction of new technologies, it is becoming more efficient and effective
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In the pharmaceutical industry, proper drug submission management is crucial to the success of any drug development process. The submission
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PMRA Annual Fees reduced for Reporting and Applications: Health Canada is implementing a new approach beginning April 1, 2023. The
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Introduction: Submitting a new drug to Health Canada can be a complex and time-consuming process. This post will provide
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Many drug industries are working in every country. To sell any OTC drug in Canada is not possible without
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Overview Manufacturers of prescription and non-prescription drugs are required to obtain a Drug Identification Number (DIN) before the drug product
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BACKGROUND Originally implemented in 1920 after the inception of the Federal department of Health in 1919, the Food and Drugs
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