Our workshops will help you update your knowledge and skill in the latest Good Manufacturing Practices, quality assurance basics, validation and auditing.
Our instructors are carefully selected from industry to ensure you receive the most current material available.
Part-time Studies courses are being offered in either of the following four formats: Online, Flexible, In-person, Hybrid. Click Availability below to see current offerings.
This workshop is an introduction to process validation. Because process validation is a critical component of the FDA approval for pharmaceutical manufacturing, it is important to know the requirements, how to prepare your protocol, how to apply in-process testing, how to identify critical steps in the process and what are the acceptance criteria.
Ancillary fees will be added at checkout for program-based courses. Fees will vary based on the number of course registrations. Learn more about ancillary fees for part-time studies.
This is an introduction to equipment cleaning validation and how to reduce the work involved in validating the cleaning of every product. A matrix approach will be discussed to help participants in their approach to cleaning validation.
Ancillary fees will be added at checkout for program-based courses. Fees will vary based on the number of course registrations. Learn more about ancillary fees for part-time studies.
Good documentation constitutes an essential part of the effective pharmaceutical quality system. During their inspections of manufacturing sites, regulatory inspectors often spend much time examining a company's documents and records. This workshop focuses on the GMP requirements for documentation and records, types of documents needed in pharmaceutical industries and record retention and keeping practices.
This workshop is recommended for individuals needing additional expertise in developing, implementing, and managing documentation systems at pharmaceutical manufacturing sites.
Ancillary fees will be added at checkout for program-based courses. Fees will vary based on the number of course registrations. Learn more about ancillary fees for part-time studies.
Auditing is a dynamic part of any pharmaceutical operation. Quality audits are one of the main tools of the Quality Management System to check the status of compliance with the applicable regulations.
This workshop introduces the participants to various types of quality auditing in the pharmaceutical industry. It presents the essential competencies required to support regulatory inspections and perform GMP self-inspections effectively. Recommended for individuals wanting to develop additional GMP Auditing expertise.
Ancillary fees will be added at checkout for program-based courses. Fees will vary based on the number of course registrations. Learn more about ancillary fees for part-time studies.
The starting point in the career development process is identifying your skills, values, interests, and preferences to determine what positions are of interest and would be a good fit. This workshop introduces the participants to essential career planning tools and techniques, including self-assessments, job search strategies, resume writing and interview skills. Recommended for individuals planning their first job or contemplating career development in the pharmaceutical industry.
Ancillary fees will be added at checkout for program-based courses. Fees will vary based on the number of course registrations. Learn more about ancillary fees for part-time studies.
For questions related to this program or its curriculum, please connect with our academic team.
Ramya Kottapalli
Program Assistant
Ramya.Kottapalli@senecapolytechnic.ca
416.764.0975
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