Management Today Women in Leadership Power List 2024.
Chief Executive, Chief Disrupter, and Chief Navigator. Sticky floor? Trampled. Glass ceiling? Shattered. I can and I did one step at a time!
If you are interested in preparing for the Diploma in Pharmaceutical Medicine examinations or just interested in learning more about pharmaceutical medicine, check out the training program 👇🏾
Faculty of Pharmaceutical Medicine
What medicines should be in my portfolio❓
When clients come to us, this is often the key question they need to answer.
Thankfully, it’s a problem we can help solve! 💪
Our Pharmly platform combines insights from a range of high-quality datasets including prescribing, dispensing, pricing and licensing to provide the answer.
This helps our clients thoroughly understand market activity to maximise pharmaceutical portfolio success. 🚀
If you’d like a demo to see how Pharmly could help power your decision-making around your portfolio, DM us and we'll be in touch!
#pharmaceuticals#pharmaceuticalindustry#pharma#dataanalytics
Join us for the next webinar in our series: An Introduction to Dry Powder Inhaler (DPI) Testing.
Ideal for those who have questions about the regulatory landscape governing DPI testing or those seeking effective troubleshooting strategies for common testing challenges, the webinar offers something for everyone.
📅 Save the date: 27th March 2024
Register now to secure your spot!
📍 10:00 AM Eastern: bit.ly/3uG4btl#InhalerTesting#DPI#Pharmaceuticals#Pharma#Formulations#WebinarWednesday
I came across this powerful quote last week, and it truly resonated with me.
"Quality is never an accident, it is always the result of high intention, sincere effort, intelligent direction, and skillful execution; it represents the wise choice of many alternatives."
This rings especially true within the pharmaceutical and medical industries. Amidst numerous choices and paths, one thing remains constant - our unwavering focus on quality and safety. It's only through high intention, sincere effort, intelligent direction, and skillful execution that we can achieve these crucial goals.
#Quality#Pharmaceuticals#MedicalIndustry
Congratulations Ann Kane and well done on this. Ann covered the following areas on this programme:
- Introduction – to pharmaceutical, (bio)pharmaceutical manufacturing in a GMP (Good Manufacturing Practice) regulated environment, quality systems, regulation and validation
- Industry regulations and guidelines for GMPs – including, FDA GMPs for the United States, EMA GMPs for European Union, ICH, and PICs GMP regulation
- FDA medical device rules – medical device regulations & and guidelines
- GMPs vs ISO 9001:2015 – what’s the difference and why we use both
- Process validation and documentation – design and verification of manufacturing systems
- Key manufacturing technologies – such as organic chemical synthesis, biopharmaceutical manufacturing, tablet manufacturing and aseptic and sterile manufacturing
- Supporting technologies – such as purified water generation, storage and distribution, clean steam, water for injection, storage and distribution
- Introduction to Quality Risk Management (QRM) – and the importance of risk management and the basic steps involved in its application
- Working in a cleanroom environment – layout, classification, gowning and monitoring
- Professional Writing Skills Program – This will guide you through the assignment writing process and equip you with the written communication skills you need for working in the industry
For an end-of-module assignment, Ann completed a report on the cGMPs that are required to consistently manufacture safe medicines, vaccines and medical devices for patients.
It included:
- The key requirements of a quality management system
- The cleaning validation sequence and how to determine cleanliness levels
- The documentation of a complete risk management process in terms of identifying risk, analyzing risk, evaluating risk and controlling risk.
- The typical equipment and process stages used in the manufacture of active pharmaceutical ingredients
- The generation, storage and distribution of pharmacopoeia grade Purified Water (PUW).
- The common cleanroom configuration and airflow direction that governs personnel and material flows in a biopharmaceutical manufacturing environment
Well done again on your hard work.
Join us for the next webinar in our series: An Introduction to Dry Powder Inhaler (DPI) Testing.
Ideal for those who have questions about the regulatory landscape governing DPI testing or those seeking effective troubleshooting strategies for common testing challenges, the webinar offers something for everyone.
📅 Save the date: 27th March 2024
Register now to secure your spot!
Choose a time:
📍 10:00 AM GMT: bit.ly/3T8G0gh
📍 3:00 PM GMT: bit.ly/3uG4btl#InhalerTesting#DPI#Pharmaceuticals#Pharma#Formulations#WebinarWednesday
Ready to enhance your expertise in Dry Powder Inhaler (DPI) Testing? Mark your calendars for March 27th and join our partner Copley for a webinar hosted by Dr. Clair Brooks. Gain insights into regulatory compliance, testing challenges/strategies, and more. Two time slots available!
#InhalerTesting#DPI#Pharmaceuticals#Pharma#Formulations#APSD#DDU
Join us for the next webinar in our series: An Introduction to Dry Powder Inhaler (DPI) Testing.
Ideal for those who have questions about the regulatory landscape governing DPI testing or those seeking effective troubleshooting strategies for common testing challenges, the webinar offers something for everyone.
📅 Save the date: 27th March 2024
Register now to secure your spot!
Choose a time:
📍 10:00 AM GMT: bit.ly/3T8G0gh
📍 3:00 PM GMT: bit.ly/3uG4btl#InhalerTesting#DPI#Pharmaceuticals#Pharma#Formulations#WebinarWednesday
