Event content
CPHI North America 2023
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Video Forecasting and Strategy – Maximizing Product Accessibility and Uptake, Improving Commercial Forecasting Skills and Analytics
As we bring in 2023, pharmaceutical companies will undoubtedly be looking ahead. But how will the events of the past two COVID years influence future aspirations? In the past, pharmaceutical companies used a mix of bottom-up and top-down processes to budget for the next fiscal year, and then made quarterly... -
Video The CDMO X-Factor: How Next-Gen CDMO Partnerships Are Revolutionizing the Pharmaceutical Industry
In The CDMO X-Factor,Andrew Carpenter, Ph.D, a leader in cGMP manufacturing of small molecule APIs, with a passion for continuous manufacturing, will challenge the boundaries of what the industry once believed possible for advanced pharmaceutical ingredients manufacturing. This engaging session will includ... -
Video Understanding Current Drivers in Drug Pricing and What this Means for the Industry
Get the inside focus on the latest drug pricing developments in the US market. Listen to the current legislator updates and how it will affect patient costs while reviewing the rising manufacturing costs from inflation and supply constraints and the market’s reaction: • Examining current manufacture ... -
Video Making a Splash in the US Market: How PBPK Modeling is Playing a Central Role in Risk Reduction in Early Drug Development
Rapid and efficient development of drug candidates is increasingly important for pharmaceutical companies with accelerated timelines and funding constraints. However, many early drug candidates have poor oral absorption properties making it challenging to achieve target pharmacokinetic (PK) profiles. Witho...
Pharmapack 2023
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Webinar Product Packaging Design & Sterilization
Packaging is an integral part of the design for pharmaceutical products and medical devices. Not only does one need to take into account the look, feel, and protective qualities of the packaging but design must be considered when determining the sterilization technology. Determining the sterilization techn... -
Webinar De-risking combination product development for large volume biologics: a pharma partner’s perspective
Transitioning drugs from IV to subcutaneous (SC) delivery brings new requirements and impacts program considerations for combination product development. In this session, we identify trade-offs that pharma weighs to de-risk combination product development programs involving large volume subcutaneous (LVSC... -
Webinar NFC & RFID Technologies: Adding Value to Drugs and Medical Devices with Connectivity
Connecting medication and medical devices to the internet can enhance product protection, improve patient safety and outcomes, and optimize processes along complex supply chains. NFC-RFID technologies are increasingly used to provide connectivity benefits more securely and efficiently, ensuring that pharma... -
Webinar Solving the Pre-Filled Syringes Mystery for Low Temperature Applications (-80°C)
New therapeutic treatments or prophylactic vaccines rely on more complicated drug formulations, often based on biologics. These drugs are highly sensitive and might require low temperature storage to keep them stable over shelf life. These extreme cold supply chain processes, something up to -80°C, provide...
CPHI Frankfurt 2022
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Webinar Keynote: Julien Tremblin, General Manager Europe, Terracycle
Julien Tremblin, European GM of TerraCycle, an innovator in sustainability solutions, shares how companies large and small can drive change, in and out of the pharmaceutical industry and how retailers, brands and consumers are reacting, pushing and adopting as they transition from linear to circular soluti... -
Webinar Why Biopharma CDMO Companies Must Transition with Long-Term Sustainability in Mind
Today, leading companies are not only centered on creating values, but they also focus on developing strategies to foster a company's longevity. Therefore, many companies have become more engaged in sustainable activities to make progress and are now joining the race. Acknowledging the importance of sustai... -
Video The Application of EXCiPACT GMP Standard To Pharmaceutical Auxiliary Materials
EXCiPACT is extending its certification scheme to PAMs and is developing a guide for manufacturers and auditors.
As these materials may be in intimate contact with a material which will be administered to patients, they should be manufactured in accordance with GMP principles. Typically, PAMs ar... -
Video Transforming Pharmaceutical Supply Chains with Synthetic Biology
Antheia is a synthetic biology company developing rapid-response biomanufacturing processes for Active Pharmaceutical Ingredients and Key Starting Materials. In this session, Christina Smolke, PhD, CEO and co-founder of Antheia will dive into synthetic biology as a manufacturing technology and its potentia...
Pharmapack Europe 2022
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Webinar Top Strategies for Environmental Sustainability with Examples
In this webinar, originally broadcast as part of the Pharmapack Europe show, Tom Oakley, Director of Drug Delivery Device Development, Springboard discusses 'Top Strategies for Environmental Sustainability with Examples'. Environmental sustainability is the defining challenge of our time. Whereas most glob... -
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... -
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).
CPHI North America 2022
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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 Panel: Major bottlenecks – Skilled Workforce, Product Quality, Manufacturing Capacity, Cost and Speed to Market
Join our panel discussion, where out experts will conduct a deep dive through the challenges in drug manufacturing. Key discussion points include: Bottlenecks in skilled workforce and what can be done to overcome this Assessing the challenges in both product and manufacturing quality and identifying... -
Webinar Strategic Manufacturing Development for Cell Therapy Products
This discussion will focus on four critical areas for process development and overall product life cycle management: Quality, Scalability, COGS and Sustainability Strategies for accelerating process development in efforts to initiate clinical trials quicker will also be discussed Examples, from both ... -
Webinar Manufacturing of Cell and Gene Therapies – Challenges and Opportunities
This presentation will focus on: The complexities of bioprocessing and manufacturing of biologics to provide a roadmap for development of effective Efficient and scalable processes and platforms that can be adopted successfully to provide patients wide access to cell and gene therapies. This session...
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