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Parenteral Drug Association - PDA The Parenteral Drug Association (PDA) is the leading global provider of science, technology, and reg

Join us for the Characteristics of Pharmaceutical Elastomers and Aluminum Seals in Parenteral Packaging Systems Training...
10/06/2026

Join us for the Characteristics of Pharmaceutical Elastomers and Aluminum Seals in Parenteral Packaging Systems Training Course!

📆10 - 11 Nov 2026
đź“ŤMiddletown, DE

Pharmaceutical elastomers are commonly applied in the form of stoppers, plungers, and O-rings for parenteral drug-delivery applications. Here, good sealing is an apparent property for effective drug containment; however, there are several other critical attributes that govern the selection of an appropriate elastomeric component for safe and efficacious drug-delivery.

In this two-day training course, you will gain insight into the fundamentals of pharmaceutical elastomers with practical considerations. Industry experts will describe component selection strategies, review manufacturing technologies, component processing and sterilization techniques. There will be a focus to understand the origin of defects and analytical tools applied for their characterization.

Learn More and Register Today: https://hubs.ly/Q04zl4kN0

“Connecting People, Science and Regulation®” is PDA’s global goal—and it starts with a strong community.By bringing toge...
10/06/2026

“Connecting People, Science and Regulation®” is PDA’s global goal—and it starts with a strong community.

By bringing together industry, regulatory, and academic professionals from around the world, PDA helps advance bio/pharmaceutical manufacturing through shared science, technology, regulatory insights, and innovative ideas.

Join PDA today and gain access to:
🔹 Critical technical information and resources
🔹 Opportunities to connect with industry and regulatory leaders
🔹 A global network of professionals and thought leaders
🔹 Opportunities to volunteer, contribute, and make an impact
🔹 A chance to help shape the industry events and technical resources of tomorrow

Become a PDA member and be part of the community advancing the future of bio/pharmaceutical manufacturing.

Learn More: https://hubs.ly/Q04wZ01l0

Need to strengthen your visual inspection program? 📍 Durham, NC 📅 October 28-29, 2026 🌟 Learn from industry experts duri...
10/05/2026

Need to strengthen your visual inspection program?

đź“Ť Durham, NC
đź“… October 28-29, 2026

🌟 Learn from industry experts during this focused, hands-on training designed specifically for compounding professionals!

Join PDA's Visual Inspection Training Course to improve your visual inspection program, identify defects with confidence, and enhance product quality through proven inspection practices.

Topics include:
🔹 Visual inspection program fundamentals, including inspection station setup and personnel selection, training, and qualification
🔹 Defect identification and classification
🔹 Human factors and common inspection challenges
🔹 Regulatory expectations and industry best practices

Using real-world examples, hands-on exercises, and interactive discussions, participants will gain practical skills to strengthen inspection processes, improve defect detection, and support the consistent delivery of high-quality compounded drug products.

Register Today: https://hubs.ly/Q04zdK4q0

Upcoming Training!Artificial Intelligence in FDA-Regulated Manufacturing Training Course(PDA 226)📆20 - 21 October📍Bethes...
10/05/2026

Upcoming Training!

Artificial Intelligence in FDA-Regulated Manufacturing Training Course
(PDA 226)

📆20 - 21 October
đź“ŤBethesda, MD

Learn how to evaluate and implement AI confidently in GxP-regulated environments. Designed for quality, regulatory, and technical operations professionals, this practitioner-led course combines regulatory guidance with seven hands-on workshops. AI or programming experience is not required.

By the end of the course, you will leave with a personalized AI implementation roadmap ready to present to your organization’s leadership.

Learn More: https://hubs.ly/Q04yDzgc0

PDA Journal Articles Wanted!Are you advancing innovation in pharmaceutical science or biopharmaceutical technology?The P...
10/05/2026

PDA Journal Articles Wanted!

Are you advancing innovation in pharmaceutical science or biopharmaceutical technology?

The PDA Journal of Pharmaceutical Science and Technology invites researchers, industry professionals, and thought leaders to submit original manuscripts that contribute to the evolving landscape of drug development, manufacturing, and regulatory science.

Submit your manuscript: https://hubs.ly/Q04wZ1440

10/02/2026

We’re excited to welcome you to Palm Springs next week for the PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2026!

Can’t make it this year? Stay tuned to our social channels for live updates, session highlights, and key takeaways throughout the conference.

We can’t wait to see you next week for an incredible learning and networking experience. Safe travels, and we’ll see you in Palm Springs!

Upcoming Training!Aseptic Processing Training Certificate Program(PDA 100)📆12 - 16 October📍Bethesda, MD Strengthen your ...
10/01/2026

Upcoming Training!

Aseptic Processing Training Certificate Program
(PDA 100)

📆12 - 16 October
đź“ŤBethesda, MD

Strengthen your expertise in sterile manufacturing with the Aseptic Processing Training Certificate Program (PDA 100). This intensive five-day program combines expert instruction, real-world case studies, interactive workshops, and hands-on activities covering contamination control, cleanroom practices, environmental monitoring, aseptic techniques, and evolving regulatory expectations.

Register today to build practical skills and earn a Certificate of Completion in Aseptic Processing.

Learn More: https://hubs.ly/Q04yD8kK0

Volunteer OpportunitiesPeer Reviewers Needed: PDA Points to Consider for the Manufacturing of ATMPs (Part 2)This opportu...
10/01/2026

Volunteer Opportunities
Peer Reviewers Needed: PDA Points to Consider for the Manufacturing of ATMPs (Part 2)

This opportunity is to serve as a peer reviewer for a New Points to Consider on Manufacturing of ATMPs (Part 2) of published PtC #14. The scope of this PtC is ATMP GMP Manufacturing requirements.

PDA technical documents rely on the contributions of subject matter experts from the industry. PDA technical documents undergo external review to provide high quality, valuable resources for the pharmaceutical industry. Authors from all levels of experience and geographies are encouraged to participate to ensure the documents are accessible and relevant to a wide audience.

Learn More: https://hubs.ly/Q04yD4BL0

Want to lead change more effectively within your compounding organization? đź“Ť Seattle, WA đź“… November 17-18, 2026 Join PDA...
09/30/2026

Want to lead change more effectively within your compounding organization?

đź“Ť Seattle, WA
đź“… November 17-18, 2026

Join PDA's Change Management for Drug Compounding course and learn practical strategies for implementing change, driving adoption, and sustaining improvements in complex regulated environments.

đź’ˇ Learn from industry experts and gain tools you can immediately apply to your organization.

Topics include:
🔹 Principles of effective change management
🔹 Change Management vs. Change Control in a CGMP environment
🔹 Assessing change impacts and organizational readiness
🔹 Stakeholder engagement and communication strategies
🔹 Sustaining improvements and supporting the full change lifecycle

Through real-world examples, interactive discussions, and practical exercises, participants will develop the skills needed to successfully navigate organizational change while maintaining compliance and operational excellence.

Register Today: https://hubs.ly/Q04yMt1B0

Attending the PDA Pharmaceutical Microbiology Conference 2026?Go beyond theory at the PDA Microbial Data Deviation Inves...
09/30/2026

Attending the PDA Pharmaceutical Microbiology Conference 2026?

Go beyond theory at the PDA Microbial Data Deviation Investigations Workshop 2026 taking place 28-29 October.

Through a start-to-finish case study, hands-on exercises, and collaborative problem-solving, you will practice conducting scientifically sound, compliant, and inspection-ready investigations. Build practical skills in root cause analysis, batch impact assessment, CAPA development, and defensible documentation.

Register Today: https://hubs.ly/Q04yt2t30

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4350 East West Highway
Bethesda, MD
20814

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Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm

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