QP Pharmaceutical Formulation and Processing Part 1 - Practical Laboratory Day

Foundational Formulation Principles and Practical Applications for Aspiring Qualified Persons

The Qualified Person should have a thorough knowledge of formulation and processing of the medicinal products they are asked to certify. The comprehensive six-day course is split into two parts, with Part 1 focusing on foundational formulation principles.  

 

Attendees will gain an understanding of preformulation studies, bioavailability considerations and the effects of excipients on physical and chemical stability. Each major product category is covered in detail, with respect to common formulations and processing techniques. 

 

The course also includes practical exercises on typical situations, allowing trainee QPs to enhance their decision-making skills using real life scenarios. Sessions will also focus on other key areas that a QP must understand including process validation and scale-up, facility design, utilities and sterilisation processes. 

 

On the last day, attendees will take part in a hands-on practical laboratory day, where they will prepare and evaluate various formulations.  

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Duration
1 day
CPD Hours
7 hrs
Locations
  • Reading (RSSL)

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Who Should Attend

This is a crucial module for QPs who are, or who will be involved in certifying commercial or investigational batches of medicinal products. The course is most suitable for delegates with little or no prior knowledge of the subject, although it also offers valuable insights for more experienced professionals.   

Key topics

The course includes the following topics and group exercises: 

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    Introduction to formulation 

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    Raw materials in pharmaceutical products 

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    Preformulation 

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    Particle size and analysis 

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    Powder mixing and direct compression 

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    Granulation, drying and milling 

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    Lubrication and compression 

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    General aspects of solid dose forms 

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    Hard and soft gel capsules 

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    Tablet coating 

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    Oral modified release 

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    Preparation and evaluation of formulations 

Learning Outcomes

By the end of the course, delegates will: 

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    Understand the key pre-formulation data that should be available and the impact of drug properties on product development 

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    Be able to demonstrate familiarity with commonly used excipients and understand the importance of sources and quality on product performance and safety 

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    Have familiarity with formulation and manufacture of the major categories of pharmaceutical products 

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    Understand the factors that can affect content uniformity, stability (physical, chemical and microbiological) and bioavailability 

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    Understand the critical processing techniques, their limitations and critical control parameters 

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    Understand principles of process validation, scale-up and technology transfer 

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    Be able to recognise the potential sources of cross contamination and mix-ups during manufacture of pharmaceutical products 

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    Appreciate issues with storage and transportation of finished products 

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    Be familiar with key annexes in the Orange Guide relating to processing and validating of products. 

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    Know how to prepare and evaluate some of the relevant formulations through practical laboratory experience 

Elena Kabova

Elena Kabova

Elana is a lecturer in Pharmaceutical Chemistry (Teaching and Research) at the University of Reading, specialising in dosage forms and the characterisation of pharmaceutical materials. Elana holds a first-class honours degree in Chemistry and went on to complete a PhD in Pharmacy. Her primary research interests lie in X-ray diffraction techniques and the characterisation of materials.
Frequently asked questions
Yes, QP Trainee packages are available with RSSL and include a number of exclusive benefits. Contact our QP Training Advisor to learn more on trainingsales@rssl.com or by calling +44 (0)118 918 4000, and join our upcoming webinar, 'To QP or not to QP?', designed for aspiring QPs. 
Places will be available for you to book unless it states ‘Full’ next to your chosen QP Pharmaceutical Formulation and Processing course date. When this occurs, we operate a waiting list service. 
Yes, we welcome bookings from self-funding individuals. Once your booking has come through to us, we will ask you to complete a new customer form and provide a scanned copy of your photographic ID so that we can raise an account for you on our systems. 
You will need to first register yourself on our booking system by selecting the QP Pharmaceutical Formulation and Processing course date that you wish to book your colleagues onto, then:

 - Add the number of people you wish to book onto the course
 - Register yourself as the booker and complete the fields accordingly
 - Add the details of those you wish to book for
 - Complete your order. 
You will receive an automated email confirming your booking details for the QP Pharmaceutical Formulation and Processing course. 10 days before the start date, if the course is confirmed to run, you will receive another email including the final course details. If the course is to be held virtually, the online registration and joining instructions will also be included.
Usually, this 1-day QP Pharmaceutical Formulation and Processing course is delivered live by our tutor, virtually on the Adobe Connect training platform. If you are looking for in-person training only, please get in touch with the team to discuss your needs via trainingsales@rssl.com or +44 (0)118 918 4000.
Our online QP Pharmaceutical Formulation and Processing course begins at 09:00am, although we request that you login at 08:30am to ensure any technical glitches can be resolved before the start time. Please review your course confirmation email to double check the exact start time of your specific course.

For our in-person courses, refreshments are available from 08.30am, for a 09:00am start. The standard finish time is 17:00pm, though some courses will finish slightly earlier or later. If you need an exact finishing time to allow for travel arrangements, please contact us via trainingsales@rssl.com or +44 (0)118 918 4000.
Your invoice will be sent approximately 30 days prior to the course start date. If you are a new customer to RSSL, shortly after we receive your booking, you will be asked to complete a New Customer Form so that an account can be created for you on our finance system. 
Yes, companies wishing to book multiple employees on one of our standard training courses (excluding IRCA Lead Auditor courses) can benefit from our group booking discount. This discount is only applicable to bookings made for the same course on the same date. Please contact trainingsales@rssl.com with your requirements and we will be happy to provide more information on the best deal available for you. 
Yes, we offer NHS Trusts a 20% discount on ALL our courses, including our Qualified Person training programme. When booking your course/s enter 'NHS' in the discount code field so that your discount can be applied on your invoice. Please note that the NHS discount code is only valid when the booker uses a NHS email address. 
Yes, certificates of attendance are issued after we have received payment in full for the course. If you have not received your certificate, please contact your own finance department to confirm if they have sent payment to us. All certificates are issued electronically by email. 
Our classroom courses are fully catered, and we provide all refreshments. If you have any special dietary requirements, please enter these into the ‘dietary requirements’ field when creating your account. Our virtual tutor-led courses will include a 45-minute lunch break. 
What our clients say

Discover the feedback from our course alumni and learn why they chose RSSL to support their professional development. 

Great course

It was a great course and interesting to learn more about oral solid dosage forms. I particularly enjoyed the optional practical day as was a great opportunity to put into practice some of the theories we had learnt about.
Anonymous
Autolus Ltd - QA Team Lead

Very informative and useful

Very informative and useful
Anonymous
Almac

Intense but useful

The course is intense but very useful for trainee QP's
Anonymous
Rosemont Pharmaceuticals Ltd - QC Supervisor

Book Your Place

QP Pharmaceutical Formulation and Processing Part 1 - Practical Laboratory Day
03 Apr 2025
-
Reading (RSSL)
10 Sep 2025
-
Reading (RSSL)
£ excl VAT
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