Tuesday, April 2, 2024

Navigating CMC intricacies: Comprehensive Understanding in Our Workshop

Greetings!


We are excited to provide you with a more comprehensive overview of our upcoming event, Chemistry, Manufacturing, and Controls (CMC) Training, following our initial introduction. This webinar is meticulously designed to offer a profound understanding of the intricate world of CMC requirements, providing essential insights into the heart of the pharmaceutical industry.


The virtual event is scheduled on April 12, 2024 between 9:00 AM to 5:00 PM (EST).

This webinar aims to unravel the complexities of the CMC portion of a Common Technical Document (CTD). Participants will engage in an in-depth analysis of critical topics, including the role of CMC in drug development, nomenclature and characterization of drug substances, analytical methods and validation, manufacturing processes, in-process controls, process validation, stability testing, and regulatory expectations for product characterization. Additionally, we will delve into the significance and structuring of Drug Master Files and explore the components integral to the CMC section in regulatory submissions.

LEARN MORE

Our webinar is tailored for professionals deeply involved in the pharmaceutical landscape, including directors, managers, supervisors, and associates engaged in various aspects such as regulatory affairs, quality assurance, product submission, training, consultancy, clinical research, documentation and technical writing, project management, and product development.


Don't miss this opportunity to elevate your regulatory affairs knowledge and advance your career. Secure your spot today by registering online

Date and Time:

April 12, 2024

9:00 AM - 5:00 PM (EST)


How is the webinar delivered?

Live. Virtual. Interactive. Instructor-led.

REGISTER TODAY!

Interested in this workshop?

Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

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