The objective of this workshop is to provide participants with a comprehensive understanding of the importance and underlying principles of Chemistry, Manufacturing, and Controls (CMC) requirements from a regulatory perspective. Attendees will gain in-depth knowledge of the CMC section of the Common Technical Document (CTD), the required format for regulatory submissions in Canada and the EU. This workshop will equip participants with the skills needed to effectively compile and present CMC data, ensuring compliance with regulatory standards and facilitating successful submissions.
Who Should Attend
This workshop is tailored for professionals involved in regulatory affairs, quality assurance, and product development within the pharmaceutical and biopharmaceutical industries. It is particularly beneficial for those responsible for compiling and submitting CMC data, including regulatory submission specialists, technical writers, project managers, and quality control personnel. Additionally, consultants and other stakeholders engaged in the preparation of regulatory submissions will find this workshop invaluable for understanding and meeting CMC requirements.
Workshop Outline
This workshop covers the following topics:
The Role of CMC in Drug Development
Nomenclature and Characterization of Drug Substances
Analytical Methods and Validation Techniques
Manufacturing Processes, In-Process Controls, and Process Validation
Developing Specifications for Drug Substances and Drug Products
Stability Testing, Stability-Indicating Methods, and Managing Acceptable Changes
Regulatory Expectations for Product Characterization
Understanding and Utilizing Drug Master Files
Structure, Content, and Key Components of the CMC Section in Regulatory Submissions
Learning Outcomes
Comprehensive Understanding of CMC in Drug Development
Gain a thorough understanding of the role and importance of Chemistry, Manufacturing, and Controls (CMC) in the drug development process, ensuring regulatory compliance and product quality.
Mastery of Analytical Methods and Validation
Develop proficiency in selecting and validating analytical methods, as well as characterizing drug substances and products to meet regulatory standards.
Expertise in Manufacturing and Process Validation
Learn best practices for manufacturing processes, in-process controls, and process validation, including the development of robust drug product specifications.
Proficient in Regulatory Submissions and Stability Testing
Acquire skills in preparing the CMC section of regulatory submissions, understanding the structure and components, and conducting stability testing to determine acceptable changes and ensure product integrity.
All participants will receive a certificate of attendance upon completion of the workshop.
Recorded Webinar – Chemistry, Manufacturing and Controls (CMC) Training