PFAS Regulations & Pharmaceutical Packaging: Navigating the Changing Landscape
PharmaTech
MAY 18, 2025
Webinar Date/Time: Tue, Jun 10, 2025 9:00 AM EDT
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PharmaTech
MAY 18, 2025
Webinar Date/Time: Tue, Jun 10, 2025 9:00 AM EDT
PharmaState Academy
MARCH 28, 2024
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AUGUST 18, 2024
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DECEMBER 2, 2024
Some of our clients have successfully implemented strategies such as displaying supplier logos and QR codes on packaging, allowing consumers to easily access information about the ingredients and clinical results. Educating consumers about the value of branded ingredients is essential to further boost this trend.
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NOVEMBER 12, 2023
View the full webinar here or watch individual segments linked below. 6 would prevent the HHS Secretary from requiring a switching study as part of the data package to receive the interchangeable designation. View ASBM’s recent webinar on the IRA’s effects here. However, S.6 ASBM surveys of U.S. Read it here.
Express Pharma
JANUARY 10, 2025
In this webinar, hosted by Agilent in partnership with the AOAC India Section, experts explore the current landscape of PFAS contamination, regulatory frameworks, and the latest analytical solutions. To watch the full webinar and learn more about the latest solutions for PFAS detection in food, visit the link below.
Safe Biologics
DECEMBER 3, 2023
ASBM and GaBI Webinar Examines Policy Challenges to Interchangeable Biosimilars On November 30, ASBM and the Generics and Biosimilars Initiative (GaBI) hosted I nterchangeable Designation for Biosimilars- Ensuring Continuity of Patient Care: Upholding Interchangeability Status for Biosimilars.
Safe Biologics
DECEMBER 6, 2023
REMINDER: FDA Draft Guidance Would Remove Interchangeability Statement from Interchangeable Biosimilars Comments Due November 17th On September 15th, the Food and Drug Administration (FDA) released draft guidance removing the interchangeability statement from the product label/package insert. Watch clips from the webinar here.
European Pharmaceutical Review
APRIL 4, 2025
The cause of any degradation is also examined whether it results from temperature, humidity levels, or interactions with any component of the container, closure, or packaging. If degradation occurs, it must remain within the specified allowable limits.
Express Pharma
OCTOBER 4, 2023
The comparison between the existing Schedule M and the draft upgraded version (as outlined in the presentation given by Dr Eswara Reddy, JDCI, CDSCO at one of these webinars) would require considerable expenditure and time. These workshops are set to continue over the next few months.
National Association of Boards of Pharmacy
SEPTEMBER 16, 2022
One requirement that is included in Title II of the Act calls for product tracing at the package level, which had not been explored widely by the industry until recently. Be ready to receive or exchange transaction information (with specific product identifiers for each package) and transaction statements electronically.
Pharma and Life Sciences Blog
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pharmaphorum
OCTOBER 27, 2022
Webinars – Webinars, whether live streamed or on-demand, can be used for communication with HCPs, HCOs, and POs. A company is responsible for the content of webinars and should take reasonable steps to ensure the audience is targeted and well defined.
Pharmaceutical Technology
FEBRUARY 3, 2023
Compared to other dosage forms, tablets are simpler to manufacture, package, and transport. Please check your email to download the Webinar. Tablet manufacturing, which is the most common OSD form, takes an API dry powder ingredient and compresses it to form tablets, which can be coated or uncoated.
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By tracking trends in product features, packaging, and consumer demand, CI allows innovation teams to design with clarityand speed. Case Study: A plumbing fixture manufacturer used CI to benchmark competitors feature sets and innovation roadmaps.
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SEPTEMBER 1, 2022
Team Arkansas also liked the idea of webinars and a more relaxed form of communication between pharmacies engaging in the program t o “bounce ideas off of one another”, to “stay engaged,” to “network,” and to have “some semblance of accountability.”
Pharmaceutical Technology
NOVEMBER 30, 2022
A vitally important assay used across various stages of drug development and manufacturing, container closure integrity testing (CCIT) involves evaluating packaging systems to determine their ability to protect the stability and sterility of pharmaceutical products. Free Webinar. Please check your email to download the Webinar.
pharmaphorum
NOVEMBER 29, 2021
It can work more naturally for webinars or bigger, company meetings, but I’ve found it can present issues for smaller groups, where it’s important for everyone to feel involved and be able to contribute equally. iii] It’s no longer just about the company, compensation package and secondary benefits (e.g., gym membership).
Pharma Marketing Network
DECEMBER 4, 2024
Highlight your commitment to eco-friendly practices, from reducing packaging waste to sourcing ethically. Using email, social media, in-person meetings, and webinars to deliver a consistent message across platforms. Patients and providers alike value brands that prioritize the planet.
National Association of Boards of Pharmacy
NOVEMBER 6, 2024
Additionally, NABP offers educational resources such as free and low cost webinars on industry topics, blogs , newsletters from the states to their licensees, and weekly and biweekly email newsletters. This helps reduce paperwork with one streamlined application process across multiple accreditations.
pharmacy mentor
DECEMBER 3, 2023
Empowering Education : As part of our partnership, we are going to provide more valuable, unique and free education in the form of blogs, webinars, videos, articles, and more. Contact Our Team * Discounts on marketing/development packages apply to new purchases only, as per our Terms and Conditions. Watch this space.
epicur
AUGUST 8, 2023
We partner with experts to offer educational webinars that ensure you understand the impact on your practice. Watch our most recent on-demand GFI webinar with Nicole Clausen, What Every Inventory Manager Needs to Know About Compounded Medications. Our team is dedicated to helping you stay up to date on regulation changes.
Pharmaceutical Technology
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Requirements on imports, packaging, storage and circulation of medical products and devices have been eased, while continuing to uphold product requirements for efficacy and patient safety. Further details: For a first-hand account of managing clinical trials during the war in Ukraine, watch this webinar-on-demand: [1] [link].
National Association of Boards of Pharmacy
JUNE 26, 2023
Review your systems and processes for DSCSA required investigations, including package-level verification. Ensure there is a process in place to produce serialized transaction information if a federal agent, state agent, or another trading partner sends a DSCSA specified request for information.
Pharmaceutical Technology
DECEMBER 13, 2022
Secondary drying removes adsorbed residual moisture until the target value is achieved, at which point the material is secured in a moisture-free package. Learn more about the importance of accurate pressure monitoring in lyophilisation by watching the webinar below. Most of the moisture is removed during the primary drying stage.
National Association of Boards of Pharmacy
JULY 19, 2024
Gathering transaction information for recalls at the package level. In addition, NABP, along with many other pharmacy organizations, maintains the dscsa.pharmacy website that includes a number of webinars, blogs, articles and other resources that are targeted for the pharmacy community.
Pharmaceutical Technology
FEBRUARY 23, 2023
Quotient Sciences supported a standalone DCS classification and formulation development package. A recent example of this was for a compound at the candidate selection stage. Permeability was high and solubility at 24 hours in intestinal buffer was less than the expected therapeutic dose, so solubility was classified as “low”.
epicur
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Watch our on-demand webinar with VSOD to hear how collaborative care can improve your practice. From virtual wellness packages to charging for telemedicine appointments and after-hours calls like you would for office visits, embracing telehealth can be an opportunity to monetize new service models that your clients actually prefer.
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Contaminants can come from a drug substance, excipients (a drug’s inactive ingredients), solvents or water used in the process, product degradation during storage, or even in a product’s packaging.
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Engagement can lead to improvements in drug delivery methods, packaging designs, and support services that enhance the overall patient experience. This education can be delivered through various formats, such as webinars, videos, and written materials.
Safe Biologics
AUGUST 23, 2024
” From the FDA’s statement: FDA has generally recommended switching studies in the past as part of the data package needed to demonstrate interchangeability of a biosimilar; however, of the 13 approved interchangeable biosimilars, 9 were approved without additional clinical (switching study) data. policy here.
PharmaState Academy
MARCH 17, 2023
Submit The post KAM (Key Account Management Webinar) appeared first on PharmaState Academy. By filling this form, you agree to our Terms of Use and Privacy Policy.*
Pharmaceutical Technology
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According to the GlobalData report Contract Injectable Packaging Trends in the Bio/Pharma Industry , more than half (55%) of FDA drug approvals in 2021 were accounted for by injectables. During the Covid-19 pandemic, large-scale vaccine production placed unprecedented demand on the parenteral packaging industry.
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For PRISYM ID client RxSource , a Global Clinical Trial Supplies Specialist, it means being ready to partner with sponsor companies to get everything set up for a clinical trial within a week, including packaging and labeling. To find out more about the webinar and to register, visit [link] .
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In response, a debt ceiling package was signed without Medicaid work requirements, symbolizing the power of patient advocates’ voices. In submitted comments , the NHC commended CMS for its initiatives to reduce patient burdens, while also emphasizing the importance of continued monitoring and oversight to strengthen the program.
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