Event content

CPHI North America 2023

Pharmapack 2023

  • Webinar Injection Time and Usability Considerations for Self-Injection Systems, a BD Perspective

    As the number of patients managing chronic diseases continues to increase, self-injection solutions play an important role in enabling the shift towards home care. Identification of potential use errors is a critical task during device development to support patient acceptance and usability. The design of ...
  • Webinar Enabling Digital Health Solutions with the Connected BD UltraSafe Plus™ Passive Needle Guard

    Sub-optimal adherence and persistence to treatment continue to be significant challenges for both on-market drugs and investigational products in clinical development. This is especially true for self-administered medications for chronic disease patients, hence driving the need for improved treatment intak...
  • Webinar Latest Data of OXYCAPT Multilayer Plastic Vial

    OXYCAPT is a multilayer plastic vial that consists of three layers, COP/New Polyester/COP. The product has achieved excellent oxygen & ultraviolet (UV) light barrier, very low extractables, high pH stability, low protein adsorption, high transparency, high break resistance, lightweight, etc. For example, t...
  • Webinar Accelerated and Real Time Aging / Stability Studies

    The presentation will look in some detail how aging / stability studies are established and address the following • What is aging / stability? • What is purpose of aging / stability testing? • What about relative humidity? • What risks are involved? • How long is the shelf life of your prod...

CPHI Frankfurt 2022

  • Video DARC: exploratory biomarker for retinal disease

    Novai is commercialising DARC, a combination biomarker consisting of Annexin A5 conjugated to a fluorophore (Dy776). ANX776 binds to stressed/apoptotic retinal cells which are visualisable as white spots using equipment routinely used by opticians, optometrists, and ophthalmologists. The images are then an...
  • Webinar Sustainable Talent Acquisition: Where has All the Talent Gone?

    Global drug sales have now hit $1 Trillion for the first time; the R&D pipeline has doubled in the last 10 years, CDMO market is expanding at a consistent 10% YOY. The pharma industry faces countless opportunities; however, there is a problem. Business leaders are asking where has all the talent gone? qq...
  • Video Reimaging Chemistry to Improve Medicines: High Functional Excipients to increase APIs effectiveness

    In today’s world, medical innovations and pharmaceutical technology are essential drivers of human health: they open up the possibility of new treatments and subsequently act as a gateway which allows people around the world to access new medicines, improving their quality of life.

    In the produc...
  • Video Building Future Pharmaceutical Talent: Students Guide

    This session will help you understand real-world life as a student entering the Pharma industry post-pandemic. We will learn more about the role a CDMO plays in the pharmaceutical industry and the importance of hiring university and school early careers from the lens of a business leader. Finally, we will ...

Pharmapack Europe 2022

  • Webinar Radiation Technology Transfer Methodology

    In this webinar, originally broadcast as a part of Pharmapack Europe 2022, speakers from STERIS will be describing the methodology for transferring the sterilization process of medical or pharma products from one radiation technology to another (e.g. gamma to X-ray).
  • Webinar Patients are People: Why Drug Delivery Needs to Evolve the User Experience

    This session will explore the value of considering the user experience for patients and how best to build it. What does the consumer sector have to show drug delivery about creating compelling experiences and reassuring users? How can packaging guide users during their journey, from onboarding to succe...
  • Webinar Climate Neutral Polycarbonates for a Zero Carbon Footprint in Drug Delivery Devices Design

    In this webinar, originally broadcast as part of the Pharmapack Europe show, Katsuyuki Takeuchi, Associate Product Manager, Terumo Europe NV will discuss how the world, and in particular the world of Plastics needs to change its Consumption, Production and Value Creation practices. Global Challenges such a...
  • Webinar Tackling the Challenges of Cloud Connectivity

    In this webinar, originally part of Pharmapack Europe 2022, Thomas Watts, Engineering Consultant, Team Consulting discusses tackling the challenges of cloud connectivity. The electronic Product Information initiative for Medicines (ePI) aim to ease the accessibility on product information to everyone with...

CPHI North America 2022

  • Webinar Ripple Effects of Expediting Vaccine Development

    In this webinar, originally broadcast as part of CPHI North America 2022, Frances Zipp, President and CEO, Lachmann Consultants Services discusses lessons learned and best practices for these relationships that can be applied to both accelerated approvals as well as “normal” drug supply during non-pandemic...
  • Webinar Considerations in Extractables and Leachables Testing of Drug-Device Combination Products

    This presentation will provide an overview of the differences and similarities of E&L requirements between pharmaceutical products and medical devices. The key elements regarding E&L testing design of combination products will be discussed. Several case studies on the extractables and leachables testing of...
  • Webinar Bioprocessing of Hypo-immune iPSC: Toward Cost-effective, High-quality Allogeneic Cell Therapies

    Discuss strategies and methodologies to develop scalable, robust, and cost-effective manufacturing processes for allogeneic cell therapies Showcase how induced pluripotent stem cells (iPSC) are being used as renewable sources of allogeneic cancer therapies Demonstrate the criticality of GMP manufacturing...
  • Webinar Proven Framework for Managing Your Outsourcing Partner

    Outsourcing drug manufacturing is a common solution to building manufacturing capacity among drug sponsors. Developing appropriate oversight for CDMO’s is key to a successful product launch. This session will discuss key responsibilities for drug sponsors in overseeing their providers, including which r...