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:
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.
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:
The QP and pharmaceutical professionals must have a detailed understanding of these topics if they are to:
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.
On completion of this course delegates will know and understand:
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:
Multi-delegate discounts available. Discounts also offered to NHS staff and charities.
Learn how a science and risk-based approach to qualification and validation helps efficiency and product quality.
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