QP Hot Topic Webtorial

Interactive Hot Topic WebTorials: Master Real-World Problem Solving with Risk Assessment Techniques

These 90 minute interactive Hot Topic WebTorials are on-line, highly interactive Webinars where participants work through real-world scenarios designed to test knowledge, problem solve and find resolutions using risk assessment techniques. Participants can then apply new ways of thinking in their day-to-day roles. The sessions run once a month on a Friday and start at 9.30am till 11am.


Presented with a ‘progressive scenario’, and facilitated by the Tutor, attendees will be expected to solve problems in real time utilising their pre-existing knowledge and experience. By sharing best practice across a wide range of different backgrounds, dosage forms and technologies you will develop your critical thinking and decision making skills.


Find the topic schedule in course programme to see what's next

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Duration
90 mins
CPD Hours
1 hrs
Locations
  • Online

Who Should Attend

The sessions provide reinforcement to delegates who have joined our Qualified Person Training and Viva Support Programme and are primarily intended for Trainee QPs and Qualified Persons. Specifically:

 

  • QP trainees regardless as to where in the process you are
  • QP trainees about to submit their forms
  • Newly qualified QPs looking to update their knowledge and develop a network
  • Experienced QPs looking to update their knowledge and network
  • Regulatory and quality professionals impacted by the topics under discussion
  • Any manufacturing or supply chain professionals impacted by the topics under discussion


However, they are equally relevant for those needing to advance their GMP, GDP, Quality Assurance, Quality Control and Production knowledge.

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QP Webtorial details

All sessions will be scenario based and may not be limited to the topics outlined below and may also cover other topics.

In February's webinar we'll explore:

 

  • The recent MHRA updates and guidance
  • Waving goodbye to PLNI (Product Licence Northern Ireland) and PLPI (Parallel Import Licence) world as a QP
  • The ongoing impact of Brexit on the QP role

Join us in February for a discussion on validation, including why URS need to have Installation Qualification (IQ) / Operational Qualification (OQ) / Performance Qualification (PQ) included and how this links to the corporate Quality Culture

This months webinar we'll be looking at:

 

  • The QP's involvement with Good Distribution Practice (GDP)
  • Assessment of temperature excursions during distribution

In May we will be returning to the topic of validation, this time covering:

 

  • IT validation
  • Cleaning validation pitfalls and places to learn

Junes session will be focused on dealing on external suppliers including:

 

  • Vendor management
  • Performing and preparing for audits
  • The importance of Quality Control and Quality Technical Agreements (QTA)

July's session recaps the changes made to Annex 1 of the EU GMP guide for non-steriles, focusing on cleaning validation pitfalls and places to learn.

In this webinar we'll discuss the updates to the USP, including:

 

  • What the changes mean for analytical method development and review
  • The impact on data integrity compliance
  • How QP responsibilities are affected

Join us for this discussion where we will be exploring:

 

  • Supply chain changes and license impact
  • On going impact of Brexit on the QP role
  • Critical medicines and shortages
  • Recalls and the impact in the UK

In this session we will tackle Autoclaves and wet loads from different perspectives, including Annex 1, steriles and Formulation and Processing

On the last webinar of the year, we'll be looking at:

 

  • Updates from the PIC/S and ICH
  • What to expect from 2026

Learning Outcomes

Don't miss this opportunity to delve into quality topic all QPs face, ensuring you can handle VIVA scenarios from a strong knowledge bases or lead your organisation when problems arise. By joining the monthly WebTorials you will:

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    The legal requirements will be identified

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    Identification of problem areas to focus on in day-to-day operations

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    How to answer VIVA questions discussions

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    Provide tools for QPs facing similar real-life scenarios to make informed decisions for investigations

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    Network with industry experts and like-minded professionals

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    Set the agenda for future workshops

Rebecca Rutter (1)

Rebecca Rutter

Rebecca is a Qualified Person and Responsible Person with expertise in biotechnology products and the provision of support for Advanced Therapy Medicinal Products (ATMPs). She has held director positions at several prestigious pharmaceutical companies where she has specialised in setting up and running greenfield manufacturing facilities, systems, processes, supply chain and achieving strategic business milestones.

Book Your Place

QP Hot Topic Webtorial
07 Mar 2025
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Online
11 Apr 2025
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Online
25 Apr 2025
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Online
06 Jun 2025
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Online
04 Jul 2025
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Online
05 Sep 2025
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Online
03 Oct 2025
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Online
07 Nov 2025
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Online
05 Dec 2025
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Online
£ excl VAT
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Why choose RSSL?

As scientists ourselves, we’re passionate about collaboration and sharing our expertise to nurture the next generation. By helping them to develop and fulfil their potential, we can tackle 21st-century pharmaceutical scientific challenges more effectively.

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    More than 30 years of experience upskilling pharmaceutical professionals

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    Small-group training adjusted to individual learning styles and needs

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    50+ training courses accredited by recognised industry bodies

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    Combination of off-the-shelf and bespoke training packages

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    Courses and consulting led by experts in the entire pharmaceutical life cycle

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    Opportunity to share and learn as part of a diverse community