1. What's Required for Release For Supply?
What is Release for Supply (RFS) in pharmaceutical manufacturing in Australia
Know the go-to guidances from the TGA
Understand the PIC/S GMP expectations
Who is the Authorised Person?
What are the new PIC/S Annex 16 requirements?
2. Responsibilities of Key Players
What does the Authorised Person do?
What are the Sponsor's responsibilities?
What are the manufacturer's responsibilities?
Learn what needs to be in your RFS process to meet requirements
What is required with multiple manufacturing sites?
What happens when a manufacturing site is overseas?
Do you need more than one Authorised Person?
And a LOT more!
Self-directed training videos, written instructions, downloadable files and assessments covering the practical theory of auditing
A comprehensive online library of topics across with 8 modules and 41 lessons - 12 months access per trainee so they can come back to the course as many times as needed
Downloadable, industry best-practice templates that are easy to use to give you a head start
Premium, face-to-face (Zoom or onsite) training time with Kathy, covering case studies, activities and FAQs that build on the content of the online part of the course
If preferred, you can also choose to have just the online training without the face-to-face training
Flexible delivery to suit your needs - schedule a call to discuss what will work best for you!
New to release for supply and the role of the Authorised Person
New to learning about the Australian regulatory requirements for Authorised Person and release for supply
Not sure if your company is meeting the TGA expectations for release for supply
Your release process is cumbersome and takes too long
Your release process is held up by upstream causes
Have an inexperienced team or company when it comes to release of product
Want to improve your team's skillset around release for supply and leveraging activities
Want a list of things to check as part of releasing a product
Want to understand how to manage multiple sites in the manufacturing supply chain
You're going for your TGA GMP license
Kathy has over 24 years’ experience working in the pharmaceutical, medical device, and biotech industries, and many of their supporting areas such as distribution & wholesaling, secondary packaging, compounding, laboratory testing, and R&D. She specialises in helping clients achieve their compliance and/or accreditation to regulatory requirements, particularly for:
Pharmaceuticals – Good Manufacturing Practices (GMPs) with various regulators
Medical devices – ISO13485 and ISO14971
Calibration and testing laboratories – ISO17025
Quality Management Systems (general) – ISO9001.
In addition to her scientific qualifications (PhD), Kathy is a qualified project manager, trainer, technical writer and Director of QSN.
See our reviews for training and consulting.
Excellent videos, clear, concise and very informative. Kathy is a great source of knowledge and her help and advice is always invaluable for us.
Medtech
Clear structure, right level of details, up to date information, useful for any medicine manufacturers/sponsors. Catering for all customer needs with the text and video.
Medtech
GMP Pharma
Very well structured and presented nicely (as expected from a professional writer)
Kathy is a very pleasant and good communicator with efficient style!
Ready to explore QSN Academy? Start by checking out our FAQs!
Our courses are not cookie cutter products. They are intended to be flexible to meet our client’s needs for training or upskilling personnel. Courses can be delivered in a variety of ways and with the option for add-on premium face to face training. Our courses are primarily aimed at B2B teams and companies, but can also be purchased by individuals. And we can also offer combinations of courses for specific client needs. All of these moving parts are assessed on a case-by-case basis for each client during the scheduled call. Consequently, prices may vary depending on client needs.
No. The scheduled call is only to establish your specific training needs and what would work best for your circumstances. As part of the discussion on the call, you may choose to proceed with requesting an invoice for the recommended training solution, or not. You may also choose to not proceed with buying the training solution once an invoice is sent to you. Please just let us know that you no longer wish to proceed with the purchase.
We will send B2B clients an invoice for payment of the training solution agreed in the scheduled call. Individuals wanting to buy an online course for their own use will be sent a link where they can pay using a credit card.
Online access to courses is available once payment is made.
Access to online courses is for 12 months.
We recommend using the Google Chrome browser for accessing online content.
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We will organize a mutually agreed date with you for delivering premium training sessions once payment is made.
Yes. Downloadable files attached to online courses or used during premium face-to-face sessions may be used by you for in-house/internal training or developing your own training materials as part of your QMS. Video content must not be downloaded or copied. Courses, training materials and files must not be shared with others outside of your company. QSN reserves all rights to our content.
Yes. You will receive an email when you successfully complete the online course assessment. That email will contain a link to download your certificate of completion. If you do not receive an email, please check your junk folder or reach out to support@qualitysystemsnow.com.au.
Yes. Some online courses are activated to allow you to post questions to the instructor from online lessons. You may also email us at support@qualitysystemsnow.com.au.
Online courses are non-refundable if you or your team have been given access to a course. Face to face premium training costs may be refunded within 10 days of purchase. However, any customizations to premium training content requested by you will not be refunded.
Yes. You will have continued access to the course materials for 12 months even after completing the course.