PDA - Parenteral Drug Association

The PDA Week 2025 Call for Abstracts deadline is fast approaching! PDA Week is the premier industry event to showcase innovative ideas, cutting-edge technologies, and real-world best practices. We invite you to submit future-focused abstracts that feature new and emerging trends, case studies that highlight successful strategies and practical solutions to real world problems and thought leadership topics that reveal the industry’s future. Topics that we are looking for include: ? Advanced Therapy Medicinal Products (ATMPs)/Biopharmaceuticals ? RAQ (Regulatory Affairs and Quality) ? Manufacturing Science ? Deadline to submit: 29 September? We look forward to reviewing your submissions! For more information: https://bit.ly/3WU3eZO Submit Abstract: https://bit.ly/4dvKPYx

Don't miss your last chance to submit your abstract! Maximize your visibility by presenting a podium or poster presentation at PDA Week 2025. Leverage this unique opportunity to highlight your work both in person and online. Topics that we are looking for include: ? Advanced Therapy Medicinal Products (ATMPs)/Biopharmaceuticals ? RAQ (Regulatory Affairs and Quality) ? Manufacturing Science ?? Deadline to submit: 29 September?? We look forward to reviewing your submissions! For more information: https://bit.ly/3WU3eZO Submit Abstract: https://bit.ly/4dvKPYx

?? Call for Abstracts is Now Open! ?? We are excited to announce that submissions are now open for poster and podium presentations at the PDA Good Aseptic Manufacturing Conference 2025! This is your chance to share innovative solutions, case studies, and thought leadership on key topics in aseptic manufacturing. We're looking for abstracts on a wide range of critical topics, including but not limited: ?? Contamination Control Strategy (CCS): Implementation case studies, microbial control, and digital tools. ?? Environmental Monitoring & Quality Control: Rapid micro methods, data trending, and sterility testing. ?? Aseptic Process Simulation (APS): High-risk interventions, process simulations, and validation parameters. ?? Manufacturing: Addressing raw material shortages, sterilization integrity, and process optimizations. ?? Sustainability: Eco-design, waste reduction, lifecycle assessments, and circular economy initiatives. ?? Submission Deadline: 24 November 2024 ?? Conference Dates: 20-21 May 2025 ?? Location: Basel, Switzerland Be part of the future of aseptic manufacturing! Submit your abstract and contribute to a healthier world through excellence in pharmaceutical production. ?? Click here to view all topics of interest and additional submission details: https://bit.ly/3BjlVO3

Did you reserve your seat yet? Join us on 18-19 November 2024, for an in-depth seminar on testing methods for pre-filled syringe systems! Hosted at the Stevanato Group facility in Piombino Dese, Italy, this hands-on workshop will offer a deep dive into pre-filled syringe technologies, with practical laboratory sessions and insights into ISO-compliant testing. Led by Horst Koller of HK Packaging Consulting, this event will guide you through every stage of a pre-filled syringe's journey, from initial design to market launch. Want to know more? Check out the agenda for a full breakdown of the program: https://bit.ly/3ydVtnk

Get a behind-the-scenes look at the Alternative Microbiological Methods Workshop with Chris Murdock, PhD, CQA.

Join us in Berlin on 03 December 2024, for a one-day workshop on Visual Inspection (VI)! Organized with the PDA Visual Inspection Interest Group, this workshop will dive into the latest trends and challenges in VI, featuring expert insights from John Shabushnig (Insight Pharma Consulting) and Romain Veillon (GSK). Topics include: - Inspecting Difficult Products, such as ATMP/CGT Therapies - Acceptance Sampling Challenges for Small Batches - Updates from the A3P Particle Interest Group Don’t miss this chance to engage in meaningful discussions, network with peers, and gain practical knowledge! Plus, consider staying for hands-on training courses following the workshop. See you in Berlin!?

As the PDA/FDA Joint Regulatory Conference came to a close, Kir Henrici, CEO of the Henrici Group, shared key insights from her session "Building a Bridge: Leveraging Data Governance Towards the Adoption of Emerging Technologies."

How to Increase Manufacturing Batch Capacity by 66% in Just Six Months? Join our free webinar in partnership with Innerspace - The Simulator Company to find out! ? Industry veterans Jacob Hughes, PMP, PMI-ACP, LSSBB (Bora Pharmaceuticals, previously Emergent BioSolutions), and Chuck Gagnon (Innerspace) will guide you through a real-world case study to show how to: - Identify key problem areas - Increase productivity - Reduce deviations - Accelerate onboarding ? Register now to save your spot! #pda #innerspace

Last chance to secure your seat! If the equation SUS plus GMP results in SOS to you, then you should sign up to this two-day course taking place from 30 September - 02 October 2024 at the Sartorius Stedim Biotech facilities in G?ttingen, Germany. Here you will learn from and discuss with technical trainers and specialists, such as Dominic Parry from Inspired Pharma Training and experienced Sartorius Stedim Biotech trainer for data handling and GMP regulations, how to implement and operate single-use technologies in a GMP-controlled environment. During the optional third day, you will have a look at the manufacturing of single-use bioreactor bags and filters, which will be followed by a visit to the Sartorius Application Center. During the visit, you will be able to see and test complete process solutions, from molecule discovery to large scale biomanufacturing. Make sure you don't miss out: https://bit.ly/3Qs4rD0

?? Our PDA Annex 1 Workshop exhibition is officially sold out! Attend to gain insights into the new revision and connect with leading companies. This workshop is an exciting opportunity to engage with your peers in an interactive format to learn about the latest EU GMP Annex 1 developments. A special highlight will be distinguished regulatory presenters from the Health Products Regulatory Authority (HPRA) and the Danish Medicines Agency (DKMA) who will bring a wealth of knowledge and experience to the workshop. Register now to secure your spot and gain invaluable insights: https://bit.ly/4bUUJT6 #EUGMP #Annex1