Parenteral Drug Association - PDA

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

Instructor Highlight!Meet Kevin J. Slatkavitz, Ph.D., President & Founder of ThinkQuality, LLC.With 30+ years of experie...
08/25/2026

Instructor Highlight!

Meet Kevin J. Slatkavitz, Ph.D., President & Founder of ThinkQuality, LLC.

With 30+ years of experience across the life sciences, Dr. Slatkavitz brings real-world, boots-on-the-ground expertise in quality, GxP compliance, drug development, manufacturing, and supply chain processes. His work has helped virtual, mid-sized, and large companies, as well as CROs, CMOs, and business partners, build effective quality and compliance strategies that support measurable business success—including regulatory approvals and successful inspections.

Join Kevin for: Quality and Compliance Management for Virtual Companies

📆 17 September
📍 Washington, DC

Learn how to successfully manage quality and compliance in a virtual or outsourced pharmaceutical environment. This practical training covers GMP, GCP, and GLP responsibilities, helping participants identify high-risk areas, strengthen quality systems, and prepare confidently for regulatory inspections.

Don’t miss the opportunity to learn from an experienced industry expert!

Register Today: https://hubs.ly/Q04vbS2v0

Tomorrow is the LAST DAY to save with Early Registration!Don’t miss your chance to join the PDA Universe of Pre-Filled S...
08/24/2026

Tomorrow is the LAST DAY to save with Early Registration!

Don’t miss your chance to join the PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2026 at the discounted rate.

📆 06–07 October 2026
📍 Palm Springs, CA

Connect with global experts shaping the next generation of injectable drug delivery and explore the latest advances across formulation science, drug delivery, device development, and combination products.
Discover how science, technology, and user experience are driving safer, smarter, and more sustainable solutions.

Register by 25 August to secure the Early Registration rate!

Register Here: https://hubs.ly/Q04v3T8P0

Instructor Highlight!Meet Darius Pillsbury, Senior Consultant at ValSource, Inc. With a B.S. in Chemical Engineering fro...
08/21/2026

Instructor Highlight!

Meet Darius Pillsbury, Senior Consultant at ValSource, Inc. With a B.S. in Chemical Engineering from Tufts University and more than 20 years of experience in the biotech and pharmaceutical industry, Darius brings a wealth of real-world expertise to the classroom.

Join Darius for: Biotechnology: Overview of Principles, Tools, Processes and Products

📆 September 17–18, 2026
📍 Washington, DC

This training course is designed to provide biotechnologists and non-biotechnologists with a basic understanding of the theory, principles, techniques and potential of this rapidly moving field.

Topics covered include scientific principles, overview of tools (recombinant DNA, genomics and gene arrays, proteomics, bioinformatics, etc.), biopharmaceutical product development, biomanufacturing strategies (protein expression, fermentation, cell culture, downstream processing and purification), and types of products and their applications in medicine.

Register today and join Darius in Washington, DC: https://hubs.ly/Q04tfwpp0

Join the Premier Microbiology Gathering of 2026!When you attend the PDA Pharmaceutical Microbiology Conference 2026, you...
08/20/2026

Join the Premier Microbiology Gathering of 2026!

When you attend the PDA Pharmaceutical Microbiology Conference 2026, you'll be part of the conversations driving the future of pharmaceutical microbiology.

The conference brings together the global microbiology community to share real-world experience, emerging approaches, and regulatory insights across contamination control, modern microbiological methods, and evolving industry expectations.

What You'll Take Home
- Practical solutions you can apply immediately to strengthen contamination control and microbiological quality programs.
- A clearer understanding of emerging technologies, modern microbiological methods, and evolving regulatory expectations.
- Real-world perspectives from industry experts who have successfully navigated today's microbiology challenges.
- New connections with microbiologists, quality professionals, regulators, manufacturers, and suppliers from across the global pharmaceutical community.
- Renewed confidence to bring innovative ideas and informed decision-making back to your organization.

Learn More and Register Today: https://hubs.ly/Q04sFNhT0

Bookstore Highlight!Technical Report No. 33 (Revised 2026): Evaluation, Validation, and Implementation of Alternative an...
08/20/2026

Bookstore Highlight!

Technical Report No. 33 (Revised 2026): Evaluation, Validation, and Implementation of Alternative and Rapid Microbiological Methods

Technical Report No. 33 (Revised 2026): Evaluation, Validation, and Implementation of Alternative and Rapid Microbiological Methods (TR 33) is intended to provide guidance for the successful evaluation, validation, and implementation of alternative and rapid microbiological methods (AMM/RMM) used in the pharmaceutical, biotechnology, advanced therapy medicinal products (ATMP), medical devices, and related industries.

Get your copy today: https://hubs.ly/Q04rYZHP0

Join us for the PDA Annex 1 Implementation Workshop 2026 – US Edition!📍 08–09 October 2026📆Palm Springs, CAConnect with ...
08/20/2026

Join us for the PDA Annex 1 Implementation Workshop 2026 – US Edition!

📍 08–09 October 2026
📆Palm Springs, CA

Connect with industry peers, regulatory professionals, and leading subject matter experts for an immersive, practical workshop focused on Annex 1 implementation.

Whether you’re strengthening your Contamination Control Strategy (CCS), enhancing aseptic operations, or preparing for regulatory inspections, you’ll gain actionable insights and real-world strategies you can put into practice right away.

Through case studies, discussion, and hands‑on problem‑solving, you’ll explore proven approaches to:

🔹 Aseptic Process Simulations (APS)
🔹 Barrier Technology
🔹 Contamination Control Strategy (CCS)
🔹 Drug Substance Manufacturing
🔹 Pre-Use, Post-Sterilization Integrity Testing (PUPSIT)
🔹 Risk-Based Material Transfer

This is a featured workshop following the PDA Universe of PFS & Injection Devices Conference 2026.

Learn more: https://hubs.ly/Q04tKMbb0

“Connecting People, Science and Regulation®” is PDA’s global goal—and it starts with a strong community.By bringing toge...
08/19/2026

“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/Q04tsqYw0

Instructor Highlight!Meet Tiffany A. Baker, MBA, Senior QRM Consultant at ValSource, LLC.Tiffany specializes in developi...
08/19/2026

Instructor Highlight!

Meet Tiffany A. Baker, MBA, Senior QRM Consultant at ValSource, LLC.
Tiffany specializes in developing and implementing innovative approaches to Quality Risk Management (QRM), designing QRM programs, fostering risk-focused cultures, and developing risk-based approaches to support contamination control strategies.

Join Tiffany for the Fundamentals of Quality Risk Management Training Course!

📆 September 17, 2026
📍 Washington, DC

This practical training will go beyond QRM concepts to explore tools, templates, facilitation tips, team management, bias, risk registers, decision-making, and best practices for building a successful QRM program within your organization.

Don’t miss the opportunity to learn from an experienced QRM professional and bring practical strategies back to your team!

Register Today: https://hubs.ly/Q04tfDXL0

Have you submitted your abstract yet? PDA Week 2027 is coming to Raleigh, NC, March 14–18, 2027. For the first time, the...
08/19/2026

Have you submitted your abstract yet?

PDA Week 2027 is coming to Raleigh, NC, March 14–18, 2027. For the first time, the PDA Annual Meeting, PDA Miniverse Conference, and PDA Visual Inspection Forum will take place together, bringing the latest advances in biopharmaceutical manufacturing, quality, medical devices, and innovation to one destination.

Abstract submissions are now open. Share your research, innovative technologies, case studies, lessons learned, or real-world solutions through a podium or poster presentation.

Contribute to one of three events:
- PDA Annual Meeting 2027
- PDA Miniverse: Medical Devices, Combination Products and Connected Health Conference 2027
- PDA Visual Inspection Forum 2027

❗Abstracts are due 31 August

Learn more and submit your abstract: https://hubs.ly/Q04sFNT-0

PDA Journal peer reviewers needed!The PDA Journal of Pharmaceutical Science and Technology is currently seeking qualifie...
08/18/2026

PDA Journal peer reviewers needed!

The PDA Journal of Pharmaceutical Science and Technology is currently seeking qualified professionals to join our pool of peer reviewers.

Serving as a reviewer is a valuable opportunity to:
• Contribute to the advancement of pharmaceutical science
• Stay at the forefront of emerging research and industry trends
• Share your expertise with a global community of professionals

If you’re passionate about supporting scientific excellence and would like to get involved, we encourage you to sign up to become a reviewer here: https://hubs.ly/Q04tltV90

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