PDA - Parenteral Drug Association

PDA - Parenteral Drug Association

Pharmaceutical Manufacturing

Bethesda, Maryland 66,175 followers

Connecting People, Science and Regulation®

About us

The Parenteral Drug Association (PDA) is the leading global provider of science, technology, and regulatory information and education for the pharmaceutical and biopharmaceutical community. Founded in 1946 as a nonprofit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance science and regulation through the expertise of its more than 10,500 members worldwide.

Website
pda.org
Industry
Pharmaceutical Manufacturing
Company size
11-50 employees
Headquarters
Bethesda, Maryland
Type
Nonprofit
Founded
1946
Specialties
Pharmaceutical Education and Training, Pharmaceutical Events, Pharmaceutical Guidance Documents, and Pharmaceutical Professional Community

Locations

Employees at PDA - Parenteral Drug Association

Updates

  • We are excited to invite you to the upcoming PDA Visual Inspection Workshop on 03 December in Berlin, Germany! This one-day event, organized by the PDA Visual Inspection Interest Group, is a must-attend for professionals involved in visual inspection (VI). With a focus on hot topics like difficult-to-inspect products (DIP) in ATMP/CGT therapies, AQL inspection for small batches, and the latest updates from the A3P Particle Interest Group, this workshop is designed for maximum discussion and practical exchange. Don't miss the chance to engage with experts like John Shabushnig and Romain Veillon, who will share their insights and moderate discussions on the current state of VI technologies. Plus, enhance your learning with hands-on training courses immediately following the workshop on 04-05 December in the same venue! Let’s connect, share experiences, and elevate our understanding of visual inspection together! 👉 https://bit.ly/4eoaLWY

    • No alternative text description for this image
  • Don't miss out on our Alternative Microbiological Methods Workshop following the PDA Pharmaceutical Microbiology Conference next week! 📆 09-10 October 2024 📍 Washington, DC Navigate the evaluation and adoption of rapid and alternative microbiological methods, focusing on emerging and alternative technologies and innovations that will push the industry forward. This workshop is structured to ensure you are immersed in substance, enlightened by analysis of real-world case studies, and given the opportunity to work and engage with your fellow attendees alongside the experts. We hope to see you there! Learn more: https://bit.ly/3NahJTh Register: https://bit.ly/3zNVmQD

    • No alternative text description for this image
  • Looking forward to the PDA Fundamentals of Aseptic Processing training course on 07-08 November in Dublin, Ireland! With a comprehensive agenda covering everything from facility design to microbial contamination control, it’s the perfect opportunity for anyone in pharma to deepen their knowledge and sharpen their skills in aseptic processing. By utilizing the Virtual Reality Cleanroom Simulator to illustrate key cleanroom principles and common misbehaviors, participants will be better equipped to excel in their roles and uphold high standards in aseptic processing. Whether you’re new to the field or a seasoned professional, this event is packed with valuable insights from industry leaders. Let’s continue to elevate our standards in pharmaceutical manufacturing! 👉 Register now: https://bit.ly/4eH67TJ

    • No alternative text description for this image
  • 🚨 Join Us for the FREE PDA Webinar on Visual Inspection & Particle Control in Parenteral Drug Product Manufacturing! 🚨 🔍 Visual inspection of parenteral drug products is critical in ensuring patient safety and product quality, especially with ever-evolving regulatory standards. Are you up-to-date on the latest developments? In our upcoming PDA Visual Inspection and Particle Control Webinar 2024, industry leaders will explore the complexities of particle visibility, regulatory compliance, and the best practices shaping the future of parenteral drug manufacturing. What to expect: - An overview of the regulatory and compendial environment - Insights on challenges and innovations in visual inspection - Best practices to enhance product quality and safety 💡 Featured Speakers: Antonio Burazer, Takeda Atanas Koulov, Clear Solutions Laboratories John Shabushnig, Insight Pharma Consulting Rukman De Silva, U.S. FDA Bring your questions and have them expertly answered during the Q&A session, moderated by Roman Mathaes. 🗓️ Don't miss this invaluable opportunity to learn from industry thought leaders. Register now and join the conversation! 👉 https://lnkd.in/drKiZZhQ

    This content isn’t available here

    Access this content and more in the LinkedIn app

  • Shoutout to all pharma professionals! We are excited about the upcoming PDA Annex 1 Workshop 2024 on 05-06 November in Dublin, Ireland. This event is packed with insightful sessions on regulatory perspectives, GMP, contamination control strategies, quality risk management, decontamination and material transfer, and more, led by industry experts. This is the place to be if you’re keen on staying ahead in sterile manufacturing and regulatory compliance. Let’s connect, share knowledge, and shape the future of pharmaceutical quality together! Register now: https://bit.ly/4bUUJT6

    • No alternative text description for this image
  • View organization page for PDA - Parenteral Drug Association, graphic

    66,175 followers

    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: 01 October 7:00 AM ET🚨 We look forward to reviewing your submissions! For more information: https://bit.ly/3WU3eZO Submit Abstract: https://bit.ly/4dvKPYx

    • No alternative text description for this image
  • 🚨 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

    • No alternative text description for this image
  • 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

    • No alternative text description for this image
  • 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! 

    This content isn’t available here

    Access this content and more in the LinkedIn app

Similar pages

Browse jobs