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Pharmaceutical Formulation and Processing Training

Dates

Times

5 days

Location

Virtual Learning - 23 hrs VILT, 8 hrs self-paced

Availability

Dates

Times

5 days

Location

In-Person - York, United Kingdom

Availability

About This Course

It is important that the Qualified Person understands the principles of formulation ad processing to ensure that informed certification and release decisions are made.

This course is delivered in two parts:

Part 1 – Non-sterile products – Virtual delivery in February

This intensive, interactive pharmaceutical formulation and processing training course allows aspiring Qualified Persons and other pharmaceutical professionals to understand the key quality requirements when manufacturing capsules, liquids, topical medicines and inhalation products.

Part 2 – Sterile products – In-Person delivery in March

This intensive, interactive pharmaceutical training course provides aspiring QPs and other pharmaceutical professionals with the knowledge they need to understand the key quality requirements when manufacturing sterile products.

We teach you the important formulation requirements for each of these product types and how those requirements influence the performance of the medicine in the body. We also teach you the key processing steps in the production of these dosage forms, as well as critical quality attributes and critical process parameters. We also cover what can go wrong during the processing of medicinal products and the potential consequences to the safety, quality and efficacy of the medicine.

Once a new chemical entity has proved its potential in clinical studies, the challenge becomes formulating the compound into an effective medicine and manufacturing that medicine reliably so that safety, quality and efficacy are assured.

This course addresses two important activities of pharmaceutical formulation and processing, and provides key information on:

  • How the physico-chemical attributes of the drug and the therapeutic indication influence:
    • Route of administration
    • Dosage form
  • Assuring bioavailability
  • Methods of manufacture of the major dosage forms
  • Factors affecting suitability for use of the major dosage forms

The QP and pharmaceutical professionals must have a detailed understanding of these topics if they are to:

  • Assist in the design and implementation of relevant and effective quality systems for dosage form manufacture
  • Contribute to the risk assessment process for processing changes and unplanned deviations
  • Assess the adequacy of cleaning strategies and validation activities
  • Assess the potential impact of changes to physical and chemical attributes of starting materials

This course is approved by the Royal Society of Chemistry as suitable for its members’ continuing professional development.

NSF's A-Z of Sterile Products Manufacture course can be used as an alternative to the Pharmaceutical Formulation and Processing Part 2 training if you're working towards gaining QP eligibility and this course's dates and/or delivery method are not suitable. Courses cover the same core content. View dates.

Key Learning Objectives

On completion of this course delegates will know and understand:

  • The principles of drug design and formulation and the impact of even minor modifications on bioavailability/bioequivalence
  • The various processes involved in the manufacture of major dosage forms, e.g. tablets, capsules, oral liquids, topical liquids, creams and ointments, sterile products and inhalation products
  • The Good Manufacturing Practice (GMP) issues and challenges for the QP to enable informed release decisions
  • How to apply the knowledge to:
    • Risk management
    • Risk assessment
    • Problem solving and decision making
    • Auditing
  • The principles of technology transfer and process validation

Course Outline

Part 1

  • Pre-formulation issues and product development
  • Routes of administration
  • Non-sterile dosage forms: Tablets, capsules, inhalation products, liquids, creams and ointments:
    • Major processing methods
    • Formulation challenges for each route of administration
    • Critical process steps
    • Key GMP requirements
    • What goes wrong and the role of the QP
  • Principles of technology transfer
  • Principles of process validation and control

Part 2

  • Design, qualification and operation of cleanrooms
  • Pharmaceutical water systems
  • Methods of sterilization and aseptic processing
  • Formulation considerations
  • Major processing methods
  • Critical process steps
  • Risk-based decision-making and the role of the QP
  • Key GMP requirements, Annex 1 and the contamination control strategy

Who Should Attend

The Aspiring Qualified Person

  • Our pharmaceutical formulation and processing training course is generally considered as the best available and our QPs are held in high regard in the industry.
  • As well as being accepted in the UK, our training courses are well known and accepted by several EU countries including Ireland, the Netherlands, Austria, Hungary and Malta.
  • You are more likely to become a QP with us than with any other training provider.
  • Pragmatic training by experienced consultants supported by key academic staff from the University of Strathclyde, one of the UK’s top schools of pharmacy.

The Pharmaceutical Technical Professional

  • Not all the people attending these courses intend to become QPs. Many use the training to develop as technical managers in other areas of pharmaceutical manufacture and control.
  • Many industry professionals from a range of disciplines attend the courses as part of their continuing professional development. Taken with some of our other QP modules, this course is designed to lead to postgraduate certificate, diploma and MSc qualifications.

Course Tutors

Each course tutor has a minimum of 25 years’ hands-on experience in the manufacture of every major dosage form. APIs, biologics, tablets, liquids, creams, ointments, sterile as well as non-sterile dosage forms – you name it, they have made it.

Course tutors will be selected from the following:

Part 1:

  • Catherine Kay
  • Samantha Clack
  • Tony Mayhall
  • Vicky Baulch
  • Richard Kettlewell
  • Luis Bimbo – University of Strathclyde

Part 2:

  • Darren Jones
  • Phil Rose
  • Ian Harwood

Discounts

Multi-delegate discounts available. Discounts also offered to NHS staff and charities.

Qualified Person Training With NSF

Watch the video
  • Having very little experience in this area I found the content to be excellent. The module was interactive and stimulated lots of interesting discussion. As always the tutors were excellent.
    Ashley Massey
    Almac, UK
  • I have enjoyed thoroughly the second part of the course. Great to summarize content knowledge and learn new aspects around formulation. Teamwork exercises are invaluable.
    David Pysznik
    Baxter Healthcare, UK
  • Great delivery of material. Lecturers made a difficult topic enjoyable and digestible.
    Jonathan Luter
    Reckitt Benckiser, UK

Additional Recommended Courses

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This highly focused, intensive four-and-a-half-day course, taught by leading scientists and former Quality Control Managers, is designed to provide the aspiring Qualified Person or pharmaceutical quality professional with the knowledge and understanding they need to be able to perform their duties with skill and competence when interacting with the Quality Control laboratories.

We will explain to you the strengths and limitations of analysis and specific analytical methods, we will advise you on how to apply the principles of quality management and GMP to the testing environment in a pragmatic, effective way, and we will advise you of the very latest “hot topics” with the regulators and how to ensure that your laboratories are in compliance.

This virtual blended training course will be delivered via a combination of an instructor-led virtual classroom and self-paced learning online. This will require an element of learning to be completed prior to the virtual classroom, as well as afterwards and this will be managed through our online Learning Management System. Full details, including timings for the instructor-led virtual classrooms, will be emailed following registration.

Tutors: Dave Waddington, Oona McPolin

Price: £3555 excluding VAT (where applicable)

Course registrations will close 5 working days before the start of the course.

You can view our booking terms and conditions from here.

Multiple Delegate Discounts are available for delegates from the same company attending the same course.
The first delegate must pay full price. The second delegate will receive a 20% discount. The third and any subsequent delegates will receive a 50% discount. Charities, NHS staff are entitled to a 50% discount. (Proof will be required).

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