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Thursday 21st March 2024
Considering the raw materials: API & Excipients
Royal Society of Chemistry, London

Raw materials, APIs and excipients play an important role in the manufacturing of pharmaceutical products therefore it is important to assess and monitor quality of these materials throughout the product lifecycle. This symposium will present an overview of testing and risk assessment of these pharmaceutical product components throughout the life cycle and could include the key themes below:
- pharmacopoeial monographs for assessing raw materials
- regulatory perspectives (ICH Q7, ICH Q11) covering aspects for small molecules, biologics and ATMPs
- risk assessment of raw materials
- Good Manufacturing Practice
- physical testing including incoming receipt of API & excipients
- method optimisation and development
- stability of APIs
- supply chain impact & resilience
- sustainability

In addition to the oral presentations, a panel session is planned for additional debate with our speakers to expand on earlier discussions and include questions on topics not covered elsewhere in the oral programme. We have a shortlist of questions already but are happy to take your "Questions for the Mar-24 panel" via email to chair@jpag.org or via the guidance on our information page so we can collate additional audience questions on the theme.

The meeting is open to the submission of poster abstracts in line with the above proposed key themes, as per our guidance on the information page.



WANT TO PRESENT A POSTER?
There will be an opportunity to present posters on the broad subject area of the symposium, subject to acceptance of a submitted abstract.
Click here for details.


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Delegate fees include registration, documentation, lunch and refreshments.


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DELEGATE RATES:
Concession : £ 45.00
Member : £ 195.00
Non-Member : £ 295.00
Student : £ 45.00


If you have any questions about the meeting, please contact us: events@jpag.org.




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SUBJECT: JPAG Symposium: Considering the raw materials: API & Excipients / Thursday 21st March 2024 / Royal Society of Chemistry, London

TITLE OF EVENT: Considering the raw materials: API & Excipients

DATE OF EVENT: Thursday 21st March 2024

EVENT LINK: https://www.jpag.org/170

VENUE: Royal Society of Chemistry, London
Burlington House, Piccadilly, London W1J 0BA

VENUE LINK: www.rsc.org/locations-contacts/

ORGANISED BY: Joint Pharmaceutical Analysis Group

WEB LINK: https://www.jpag.org/

SPONSORS: Royal Pharmaceutical Society and Royal Society of Chemistry

CONTACT: Hon Events Secretary JPAG, events@jpag.org


Raw materials, APIs and excipients play an important role in the manufacturing of pharmaceutical products therefore it is important to assess and monitor quality of these materials throughout the product lifecycle. This symposium will present an overview of testing and risk assessment of these pharmaceutical product components throughout the life cycle and could include the key themes below:
- pharmacopoeial monographs for assessing raw materials
- regulatory perspectives (ICH Q7, ICH Q11) covering aspects for small molecules, biologics and ATMPs
- risk assessment of raw materials
- Good Manufacturing Practice
- physical testing including incoming receipt of API & excipients
- method optimisation and development
- stability of APIs
- supply chain impact & resilience
- sustainability

In addition to the oral presentations, a panel session is planned for additional debate with our speakers to expand on earlier discussions and include questions on topics not covered elsewhere in the oral programme. We have a shortlist of questions already but are happy to take your "Questions for the Mar-24 panel" via email to chair@jpag.org or via the guidance on our information page so we can collate additional audience questions on the theme.

The meeting is open to the submission of poster abstracts in line with the above proposed key themes, as per our guidance on the information page.

SPEAKERS:
Iain Moore - EXCiPACT asbl
Richard Smalley - Consultant and QP Assessor




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We always seek feedback from delegates attending JPAG events through an Evaluation form.

A recent analysis of the results has shown that more than 95% of attendees thought that JPAG meetings were well planned, relevant and met their main objectives, and would recommend JPAG meetings to colleagues


TESTIMONIALS...

Very enjoyable and thought-provoking day; going away with plenty of notes and specific items for discussion.

Excellent meeting, challenging and thought provoking. The organisation was excellent, thanks to all the efforts that JPAG team have made.

I have not attended a bad JPAG meeting yet. They are really good value for money and I really love to get the presentations as PDFs


I did appreciate receiving the slides before, as then I could print them and make notes around them during the symposium.

Getting an industry perspective on this topic was most helpful.

I appreciate having access to relevant JPAG seminars from overseas; provision of lectures beforehand to allow reading beforehand.

I did like having the presentations available early, with the webinar portion being focused on Q&A.

Fantastic to hear from NHS speaker, provides real insight to patient/clinician considerations that we don't necessarily see in industry.

From attendee perspective, the course did not take up the whole day as no travel necessary and overall good value for money.

Hearing the information from the clinical setting side was very useful.

Well organized. This was an amazing session. Prior sharing of the presentation was a great add on!

The most useful aspect of the webinar was the variety in the presentations across industry and the regulators. Really good to review the presentations beforehand.

Good value, well organised symposium. Always useful for focused topics.

A very good day. Enjoyed getting to speak to the presenters to discuss current challenges in industry.

Well done to all the speakers and the organisers for being able to successfully hold highly informative conferences virtually! (July 2020)



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