PDA Conference 2022 October 18-19, 2022 We are exhibiting at PDA, October 18-19, 2022 taking place in Palm Springs, USA. Innovative Methodologies to Accelerate the Development of Combination Products for Novel Drug Products Involving Delivery of High Dose High Viscosity Formulations John Lewin, PharmD, MBA, BCCCP, FASHP, FCCM, FNCS, Chief Medical Officer, On Demand Pharmaceuticals Inc. If an event is cancelled, registrants will be notified by PDA immediately and will receive a credit (registration fee paid). Michael de la Torre, CEO, Redica Systems. The successful development and commercialization of combination products requires robust partnerships between pharma, device, and component suppliers. Learn about opportunities and benefits. Cancellation requests must be emailed to [emailprotected]. Phone: +1 (760) 322-6100 10:45 12:15 | P2: Lessons in Effective Drug-Device Development Partnering Moderator: Philippe Lauwers, Director Technology Development, Terumo Pharmaceutical Solutions. Moderator: Diane M. Paskiet, MS, Director of Scientific Affairs, West Pharmaceutical Services, Inc. This session will take a look at the significant strides made in the development of gene therapies, new molecule delivery systems and CRSIPR technology. What if formulations could be synthesized when and where they are needed? Mihaela Simianu, PhD, Executive Director, Merck & Co., Inc. D2: Regulatory Intelligence in the Digital Age: Friend or Foe? Interested in becoming a sponsor? The 2022 PDA Universe of Pre-Filled Syringes and Injection Devices Conference will continue to build on the reputation of past events while bringing to light the latest advances in the field. Iain Simpson,Commercial Director, Phillips-Medisize. Los Angeles International Airport (LAX) is 124 miles from Hotel. Tel: +1 (301) 656-5900, 20 Bendemeer Rd, #04-02 BS Bendemeer Centre Singapore 339914 GENERAL TERMS AND CONDITIONS: PDA will send you a confirmation letter within one week of payment being received. With your valuable input, we can determine if there is value in having a deeper discussion (i.e., potential PDA project) around this idea of integrating, coordinating, prefabricating, or even prequalifying critical components of a facility ahead of the construction. The pandemic has changed the world of pharmaceutical packaging by bringing new, complex therapeutic entities into the mainstream seemingly overnight. Dive into exciting interactive sessions and tracks especially designed for manufacturing leaders, technical experts/scientists, and early career professionals. Tel: +1 (301) 656-5900, 20 Bendemeer Rd, #04-02 BS Bendemeer Centre Singapore 339914 Jeanne E. Moldenhauer, MS, Vice President, Excellent Pharma Consulting, B1: Process Intensification: Increasing Yield per Unit Palm Springs, CA November 08, 2021-November 11, 2021 Society for Neuroscience (SfN) Overnight Guests |$32 + tax The new Annex 1 revision was recently released! Effects of Manufacturing Date on Silicon Oil Particles in Prefilled Syringes This balance would give the pharmaceutical industry the ability to positively impact patients by offering new treatments faster. Taxi fares from PSP are approximately $10 one way, not including tip, and will take about 7 minutes. IG6: Microbiology/ Environmental Monitoring Jake Keeler, Sr. 10:45 | Device and Drug Companies on the Same Path: A Collaborative Approach to Developing a Combination Product Mary E. Farbman, PhD, Executive Director, Global Quality Compliance, Merck & Co., Inc. 11:05 | Re-Imagine Audit: Bringing GxP Auditing into the Quality 4.0 Paradigm New Materials and Advanced Manufacturing Techniques of Films for Sterile Injectables Processing and Finished Dosage Form Through a Re-engineered Supply Chain Recent developments have shown a rising preference for self-administration of drugs, in which autoinjectors have become one of the key delivery devices supporting subcutaneous injections. The filtration and sterilization presentation will provide insight into the different types of sterilization and the parameters needed to demonstrate success. The pandemic experience typified the need to be prepared for serious unanticipated events. Tel: +1 (301) 656-5900 Benben Song, PhD, Global Product Manager, Pall Corporation, 16:20 | Training is More than a Checkbox: Examples and Case Study in Training Effectiveness The 2022 PDA Annex 1 Workshops highlight critical changes in the new regulation and include interactive sessions to provide attendees with a clear understanding of and means to implement all the requirements of the rule. In the first presentation, Dr. John Ludwig will take the audience through Pfizers amazing journey in developing the COVID-19 vaccine. Current global issues like supply chain issues and drug shortages unfortunately wont come to an end tomorrow. Manager, R&D, Product Sustainment, West Pharmaceutical Services, Inc. Moderator: Shelley M. Preslar, MBA, President and COO, Azzur Training Center Raleigh LLC, 16:00 | Blended Training Approach to Minimize Human Error in Biopharmaceutical Manufacturing Peter Gompper, MSc, MBA, Co-founder, Rubitel, An Iterative Process Utilizing Real World Data Collection to Improve Support for Patients with Diabetes The Renaissance Palm Springs Hotel is located at 888 Tahquitz Canyon Way, Palm Springs, CA 92262 USA. The group rate is $199 for single or double occupancy. A block of rooms has been reserved for meeting participants at the Courtyard Palm Springs Hotel. Please contact us if you are entiteld to receive a discount. In this session, the speakers will provide insight into modern microbial methods by discussing the validation process and regulatory acceptance for an automated colony counter utilizing a cross functional industry team, navigating speedbumps throughout implementation of a biofluorescent particle counting system, and a case study on rapid microbial detection for a purified water system. This session will explore various opportunities for making home drug delivery a reality from smart delivery devices for the home setting, enabling primary containers for single use administration to patient training and on-boarding solutions specifically designed for at-home use. Palm Desert, CA. James M. Fries, CEO, Rx-360, 12:15 13:45 | Networking Luncheon, Poster Presentations, and Tech Talks in Exhibit Hall. Through unprecedented professional collaboration, tremendous progress has been achieved in technology and science over the past few years. Tibor Hlobik, Sr. Director Product Technology Services, West Pharmaceutical Services, Inc. Shear Damped Auto-injector a Novel Approach to Mitigating the Risks and Difficulties Associated with Injecting High-Viscosity & Emergency Use Pharmaceuticals If you come from a Governmental or Health Authority Institution or from an Academic Organization please contact Ms. Antje Petzholdt before registering. The rate is $249 for single or double occupancy. Statements claiming to offer our attendee lists are fraudulent. An Insight from PFS Manufacturing for AI Moderator: Laurent Jeanmart, PhD, Head for Packaging and Medical Devices, GSK, 15:45 | Hybrid Prefilled Syringes Suitable for Cold Storage Vaccines and Biologic Drugs Without Compromising Container Closure Integrity CG Global Metals & Mining Conference. This session will present impressive opportunities for the future, such as having pharmaceutical products available on demand, and a vision of potential outcomes if companies can move past the concept of wanting to be a fast second to adopting new technologies moving towards a future of going first together! Moderator: Amanda M. McFarland, MS, Senior Consultant, ValSource, Inc. Aseptic process simulation (APS) has been identified as one of the key aspects of aseptic process control and monitoring. Be sure to tell the reservationist that you are with the PDA Meeting to receive the PDA group rate. In January 2020, the first U.S. case of COVID-19 was confirmed, declared a pandemic in March, and by April, nearly half of the world's population was under lockdown. The speaker will conclude with a discussion how to apply the lightspeed paradigms for future successes. Individuals will be responsible for payment of their own cancellation fees. Max Fill Volume Evaluation for Pre-filled Syringes 48 hours| $26 Uri Baruch, MEng, Partner & Head of Drug Delivery, Cambridge Design Partnership, B2: Deep Cold Storage: How to Improve Integrity and Stability Spencer Pratt, Software Compliance and Test Manager, West Pharmaceutical Services, Inc. 10:45 |Development of a Closed-Loop Wearable Injector System for Emergency Delivery of Naloxone Reservations must be secured by Friday, 30 September 2022. Klaus Ullherr, Senior Product Manager, Syntegon Technology GmbH. The current version presents a diverse, international perspective on regulatory expectations, recommendations, and requirements for modern sterile drug and biologic product manufacturing. Unfortunately, emails are circulating that offer to sell attendee lists for many of PDAs conferences and events. Throughout the years, we have seen changes to regulatory strategies that highlight the use of emergency use authorizations in hopes of thwarting the pandemic. Bethesda, MD 20814 USA Discuss the market benefits of pre-filled syringes and injection devices; Identify critical attributes of end-user friendly devices; Explain how innovation is helping patients to have a positive experience in managing their therapies and assuring compliance to dose regime; Summarize manufacturing requirements of pre-filled syringes, injection devices, safety devices, and final drug/device combo products; Discuss quality standards, regulatory and compliance concerns; List insights through case studies presented by industry experts; and. Taxi fares from DFW are approximately $45-50 one way, not including tip. Hal Baseman, MBA, Chief Operating Officer, ValSource Inc. 08:20 | Qualification and Training Moderator: Jakob Lange, PhD, Senior Director Delivery Systems, Ypsomed AG, 08:30 | Making a Difference: Utilizing Human-Centered Design to Improve Health Outcomes Philip A. Villari, MS, Associate Principal Scientist, Merck & Co., Inc. 11:25 | A Rapid Microbial Detection Technology to Identify Water Purification Failures in Real Time This will be followed by Amgens Dr. Ronald Forster discussing the merits of developing platform technologies, and how they enable continuous improvement in the patient journey through product quality, innovation, and manufacturing efficiency. This session will focus on auditing in the new normal by providing details on various techniques and technologies for effective use in audits and inspections. Located downtown next to an iconic Dallas landmark Reunion Tower, Hyatt Regency Dallas is a gateway to the best of the city. She will verify your status and register you. For example, in viral vector manufacturing, challenges arise due to the constant balance between processing small batch sizes and ensuring the valuable product makes it into the freezer within the time that the product is still stable. 08:30 10:00 | P3 14:10 | Article 117 of the EU Medical Device Regulation: Regulatory Best Practices and Opportunities Associated with Notified Body Opinion (NBOp) Open letter to the Secretaries of State for Housing and Justice - 10/10/2022. Nitin Rathore, PhD, Executive Director, Amgen Inc. 16:20 | Advancing Cell Therapy Processing using Evolving Equipment Technologies We will highlight whats in store for the future of pharmaceutical manufacturing. All costs incurring in connection with visa affairs shall be borne by registrants. These emails are sent by scammers. Herve Soukiassian, Ass. Stefan Mangold, PhD, Manager Concept Development, Ypsomed AG, B1: Challenges and Opportunities for Moving Treatments to the Home Setting IG4: Visual Inspection Gabriele Rustici Venturini, MSc, R&D Engineer - Mechanical Designer, IMA Life, 14:10 | Selecting and Collaborating with Manufacturing Partners to Achieve Successful Product Launch For later registrations, PDA Europe will be unable to assist participants in any visa affairs. It's time to come together and celebrate all that is good about being an educator. 13:30 | An Overview of International Standards Impacting Delivery Devices, ISO TC84, and Recent Changes to ISO 11608 Series This conference will explore the future of pharmaceutical devices, such as rapid technological advances, that will push the industry ahead while bringing . Copyright Parenteral Drug Association. In this session, we will be introduced to process intensification through an application using cell-based vaccine manufacturing. Wendy Woodley, Staff Scientist II, BD. For those registered for the in-person meeting, you will receive a link to upload and verify your vaccine status in early 2022. Guangli Hu, Principal Scientist, Merck & Co., Inc. Elastomer Plungers with Fluoropolymer Barrier Films Utility for Emerging Drug Products Join Gore at the 2022 PDA Universe of Pre-Filled Syringes and Injection Devices Conference. Learn about opportunities and benefits. Steven R. Kaufman, MBA, Vice President, Drug Delivery Systems, Stevanato Group, 11:15 | Cross-Industry Collaboration as Enabler for the Rapid and Successful Development of New Injection Devices: A Patch Injector Case Study Jakob Lange, PhD, Senior Director Delivery Systems, Ypsomed AG. Visit the Gore team in the Exhibit Hall at Booth 608 to learn more about GORE IMPROJECT Plungers. Learn about opportunities and benefits. Janmeet Anant, Senior Regulatory Consultant, MilliporeSigma, C1: Vaccine and Virus Products in Focus The 2022 PDA Universe of Pre-Filled Syringes and Injection Devices Conference will continue to build on the reputation of past events while bringing to light the latest advances in the field.This conference will explore the future of pharmaceutical devices, such as rapid technological advances, that will push the industry ahead while bringing . Indulge in the ultimate relaxation at Renaissance Palm Springs Hotel. Please be aware that obtaining and canceling hotel reservations is the responsibility of the meeting registrant. Bruce Loxley, Senior GMP Compliance Advisor, GSK Vaccines, 11:25 | The Link between Patient Safety and Pharmaceutical Auditing during a Pandemic Brad Womble, Managing Director, Healthcare Strategy, Jabil, Inc. Continued advances in materials of construction, manufacturing processes, injection processes and safety devices, and other technology improvements create a dynamic environment in the drug delivery device arena. 10:45 | Data Integrity Trends in 2021 A blizzard of regulatory and quality information exists in the world of pharmaceutical manufacturing today, from both internal and external sources. This session opens our in-depth look at the content of the draft Annex 1. The aim of the 21st Century Cures Act is to enable the production of safe and effective medicines to improve patient experiences and outcomes. 13:20 | Production and Specific Technologies (Blow-Fill-Seal, Lyophilization, Single Use System, and Terminal Sterilization) Patrick Poisson,EVP, Technical Operations, United Therapeutics Corp. Attendees will discuss the implementation challenges, and what can be done to meet those challenges, associated with the topics presented in P7: Production Technologies, Part 2 (Container Closure Integrity Testing and Finishing and Production and Specific Technologies (Blow-Fill-Seal, Lyophilization, Single Use System, and Terminal Sterilization). This workshop will provide an opportunity for attendees to hear from industry experts and regulators, and open discussions with their peers challenges and best practices. If you come from a Governmental or Health Authority Institution or from an Academic Organization please contact Ms. Antje Petzholdt before registering. Paul Draper, MEng, Senior Sector Manager, Medical & Scientific, DCA Design International, 13:50 | Development of Digital Surround for Connected Devices: Real-Life Case Study Amin Sedighiamiri, PhD, Associate Director, AstraZeneca, 13:50 | Addressing Primary Container Challenges in Autoinjector Drug Delivery: Interim Results of a Multiphase Bioburden Study for a Cartridge-Based Autoinjector Sheldon Moberg, MA, SVP Drug Delivery, Bexson Biomedical, 14:10 | A Patient-Centered Approach to Development of Novel On-Body Drug-Delivery Solutions for Injectable Biologics: A Study with Multiple Target Groups Vaishali Shah, MS, Head of Quality Systems and Compliance, Kite Pharma, A Gilead Company 15:30 16:30 | P4: Equipment, Technology, and Utilities Patient-focused drug development is described in regulatory guidance as a multifaceted approach to link patient information with the product lifecycle. Unfortunately, emails are circulating that offer to sell attendee lists for many of PDAs conferences and events. Connecting People, Science and Regulation, Gov./Health Authority/Academic (Member/Non-Member), Gain awareness of the requirements and changes in Annex 1 and move towards compliance with the proposed changes in the revision, Develop strategies for implementation and verification of the Annex 1 requirements, respectively, for their organizations. PDA reserves the right to modify the material or speakers/trainers without notice or to cancel an event. 10:45 | Protocol-Based Site Internal Audit Program: A Network-Wide Case Study Cutting Edge of Aseptic Transfer Technology in Regards of ATMPs and ADCs (mAbs) If someone other than PDA or the PDA chosen hotel contacts you suggesting that they represent any PDA event, they do not. Weve come together to create effective tools to fight a global pandemic. The Parenteral Drug Association (PDA) and the U.S. Food and Drug Administration (FDA) are co-hosting the PDA Conference again this year. The Palm Springs workshop, 20-21 Oct., is the fourth sponsored by PDA in 2022. 16:25 | Evaluation of Pre-filled Syringe Container Closure Integrity at Deep Cold Storage Conditions Using a Combination of Predictive Modeling and Empirical Testing (This applies in particular to costs for submitting documents by courier.). If someone other than PDA or the PDA chosen hotel contacts you suggesting that they represent any PDA event, they do not. PDA Universe of Pre-Filled Syringes and Injection Devices Conference is starting soon and we are excited to be a sponsor of this event! Amir Genosar, CEO, Aktiv Pharma Group, Practical Implementations of the Critical Parameters Design and Management (CPDM) Process in Emergency-Use Injector Programs Importance of 2.25ml Autoinjector Rod to Plunger Design Space an Overlooked Critical Input for Dose Accuracy and Elimination of Leakage (This applies in particular to costs for submitting documents by courier.). Bethesda, MD 20814 USA Leader: Susan M. Dounce, PhD, Director Commercial Technology Development, West Pharmaceutical Services, Inc. CANCELLATION: If a cancellation request is received 30 days before the event, a credit (registration fee paid minus a 200.00 USD/EUR processing fee) will be given. Updates on ISO standards will be presented, as well as discussing ramifications and the path ahead. Ludovic Gil, R&D Engineer, BD, Human Factors Approach to Incorporating Connectivity into Medical Device Connectivity Please call 214 849 6831 for bus information. Unfortunately, emails are circulating that offer to sell attendee lists for many of PDAs conferences and events. With the rise of therapies moving from clinic to home administration, many challenges exist to make this common practice. Akshay R. Kamdar, PhD, Senior Director - Container Closure, Materials Engineering and Process Innovation, Eli Lilly and Company William G. Whitford, Life Science Strategic Solutions Leader, DPS Group, 11:05 | Process Intensification: What's Possible When Declaring an Acceptable Use of Design Space 16:00 | The Role of Psychological Safety in Reducing Human Error and Advancing Quality Management Maturity Kelvin H. Lee, PhD, Institute Director, National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL). To progress our organizations to the next level, new and innovative ways of thinking need to be employed. 13:00 14:15 | P3: Premises and Barrier Systems Thomas James, Mechanical Engineer, Key Tech B-Lot, 8-24 hours | $19 Moderator: Deborah DuFresne, Head of Pipeline and Due Diligence, Pfizer. Learn about opportunities and benefits. The Beneficial Feedback Loop of the Digital Twin Asmita Khanolkar, MS, Senior Director, Cambridge Pharma, Oval, SMC, Integration of New Technologies with Existing Systems Challenges and Opportunities 13:00 13:50 | P7: Production Technologies, Part 2 Juergen Metzger, Product Specialist, Sartorius North America Inc.. Design & Customization of Lubricants and Related Materials to Meet the Diverse Needs of the Parenteral Drug Delivery Industry Potential participants must be clients of UPS shipping agency and submit their UPS customer reference number to PDA EU (together with their registration). Consider the possibilities: Ulrich Kllisch, PhD, Manager Data Integrity, GxP-CC, 11:05 | A Deep Dive into Industry-Wide Recall Data: Leveraging an Expert Ontology and AI to Uncover Patterns and Insights If you receive emails that propose to sell PDA conference attendee lists, do not engage with the sender and delete the message immediately. Drug-Device Combination Products (DDCP) Development and Lifecycle Planning Phone: +1 (888) 236-2427. Reservations must be secured byFriday, 23 September 2022. 08:00 09:15 | P5: Personnel Training, Qualification, Gowning, and Monitoring/Assessment Regulatory requirements, industry experience, and evolving market trends are critical considerations to ensure a complete understanding of the application of pre-filled syringes or other pre-filled containers and injection devices to drug delivery. Parenteral manufacturing is an expensive and time-consuming process, with several stringent requirements needed to guarantee quality and safety of the medicine produced. It is PDA's recommendation that you book your hotel directly through the official PDA chosen hotel that is listed on our web site. In this session, we will share case studies of next generation technology implementation in both biologic drug product and cell therapy manufacturing processes. This session will take a look at some of the key design and operational aspects that have been impacted by the revised Annex 1. Moderator: Theresa E. Bankston, PhD, VP Customer Success, BD, 15:45 | Digital Healthcare in Drug Delivery: The Pillars of Hardware and Software to Empower the End User Joerg Stumbaum, Project Manager, PPS&P, Vetter Marty Coyne, BEME, MBA, Principal, Matchstick LLC, 14:10 | Integrating Secure and Easy to Handle Connectivity into a Pre-Filled Device for Automated Injection Logging Tel: +1 (301) 656-5900 Paul Lopolito, Sr. Technical Services Manager, STERIS, B3: Navigating the Realm of Microbial/Rapid Technologies through Innovation and Collaboration Toni Manzano, PhD, CSO and Co-Founder, Aizon. DART Light Rail Service: The hotel is conveniently connected to Union Station on the Red and Blue lines and is also a stop for TRE commuter rail to Fort Worth. Cancellation requests must be emailed to [emailprotected]. Check out who is attending exhibiting speaking schedule & agenda reviews timing entry ticket fees. The Hyatt Regency Dallas is located at 300 Reunion Boulevard, Dallas, TX 75207. Dallas, TX Palm m105 was a nice device for its time, it had a grayscale screen with a "stunning" 160x160px resolution and a 16 MHz Motorola CPU. Tracy Moore, Director, TM Pharma Group Ltd, 09:00 | Q&A with Additional Panelist Rob Hall, Design Team Manager - Product Design, Owen Mumford. The 2022 PDA Universe of Pre-Filled Syringes and Injection Devices Conference will be live in Palm Springs from the 18th-19th October and we're looking forward to seeing you there. The Covid-19 pandemic redirected both industry and public focus on vaccines and viral products. 2022 PDA Annex 1 Workshop (Palm Springs) Oct 20 - Oct 21, 2022 Palm Springs, CA Closed Overview Agenda Speakers Additional Information Travel Registration Fees Exhibit & Sponsorship Related Events Contact Program Highlights The new Annex 1 revision was recently released! Virtual February 28, 2022-March 03, 2022 17th Annual HD Therapeutics Conference. If someone other than PDA or the PDA chosen hotel contacts you suggesting that they represent any PDA event, they do not. Managing Software Development for an on Body Delivery System Using FDA Guidance and ISO/IEC Standards We call on the government to honour its three year promise to abolish so called 'no fault' evictions and we also call for the instatement of an evictions moratorium. The 2022 PDA Annual Meeting promises to have something for everyone! Learn about opportunities and benefits. Copyright Parenteral Drug Association. Trending and analysis of gloves and gown environmental monitoring (EM) data can provide critical feedback on individual operator performance, potential routes of contamination, specific gowning procedures, and overall training efficacy. Moderator: Guido Kremer-van der Kamp, Senior Consultant - Global BioPharm Center of Excellence, Merck Chemicals GmbH. $18. James L. Vesper, PhD, MPH, Director, Learning Solutions, ValSource, Inc. 16:20 | Is Regulatory Intelligence Compatible with an Effective QMS? Seungyil Yoon, PhD, Vice President, Drug Product Development, Samsung, 11:25 | The Top Challenges (and Solutions) to Develop and Commercialize Intradermal Drug Delivery Devices Guestroom rates are subject to State and Local taxes. Donald C. Singer, MA, Senior Microbiology Technical Consultant, North America, Ecolab Life Sciences, 13:40 | Barrier Technologies: RABS and Isolators, Glove Integrity, Robotics, Decontamination Alex Lyness, PhD, Senior Manager, Research and Technology, West Pharmaceutical Services, Inc. 11:05 | RFID Tracking for Asset Management, Compliance Support, and Process Improvement Rudolf Michael Weiss, Dipl.-Ing., Global Head of Pharma+Medical, Stubli, 07:35 | A Real-World Example of Sustainable Drug Delivery the Development of the First Reusable Pen Injector for Concentrated Insulin This session will also address the expanded scope of Annex 1 to include some non-steriles. The Interest Group will be discussing the recently launched a survey on process validation approaches. Marc Glogovsky, MS, S.M. Young Harris, GA. PDA reserves the right to modify the material or speakers/trainers without notice or to cancel an event. Jerry L. Chapman, MBA, Senior GMP Quality Expert, Redica Systems. Cheryl Stork, Scientist II, Preclinical Translation, Biora Therapeutics. All registrations which will involve visa matters will have to be submitted to PDA EU four weeks prior to the start of the event at the latest. The 2022 PDA Universe of Pre-Filled Syringes and Injection Devices Conference explores the future of pharmaceutical devices. It places a heightened emphasis on the use of risk-based assessment and approaches to design and evaluate manufacturing contamination control. [emailprotected], Tel: +49 (0) 30 43 655 08-10 For your credit card information safety: Please send your details by fax only, For an easier registration, please note the helpful hints on the registration form. After the event, Agle will sign books and the Modernism Week 2022 commemorative posters he designed, pictured above. This session will explain how to get the best internal data from personnel, will reimagine todays regulatory intelligence process from start to finish, and will make the case for disrupting the status quo by driving to a single, globally harmonized Quality Management System. The focus of this Interest Group will be to discuss different approaches and methodologies to increase our ability to cut down the time it takes to get to market. Oliver P. Stauffer, MBA, CEO, Packaging Technologies & Inspection LLC. Tel: +1 (301) 656-5900, Am Borsigturm 60 ABRF 2022, Palm Springs, California ABRF 2021, Virtual Annual Meeting (Click here to see a meeting summary from Instrument Business Outlook!) Reservations must be secured by Friday, 04 March 2022. Whether you are here to work or play, Hyatt Regency Dallas is designed to meet all of your needs. 10:15 | Aseptic Processing Moderator: Kakolie G. Banerjee, PhD, Senior Scientist, MilliporeSigma. 15:00 16:45 | P8: Aseptic Process Simulation and Environmental Monitoring For later registrations, PDA Europe will be unable to assist participants in any visa affairs. October 18-19, 2022 Palm Springs, CA Booth #606. 11:05 | Streamlining Human Factors Assessment Strategies for Prefilled Syringes Anne-Sofie Staples, MSc, Industrial PhD Student, University of Copenhagen/Novo Nordisk A/S Discuss market, industry trends and new technologies.
Small Houses For Rent In Dutchess County,
12 Gauge Customs Mirror Brackets,
Articles P