Pharmaceutical Technology

SEPTEMBER 26, 2022

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].

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The FDA Law Blog

NOVEMBER 22, 2022

Transformation (events involving manufacturing, processing, or changing a food, its packaging, or packing, not including initial packing, harvesting, or cooling, listed above). FDA will hold a webinar to provide an in-depth overview of the final rule and Q&A on Dec. 7, 2022 at 1 p.m.

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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.

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PQA

JUNE 27, 2024

Pilot participants were provided a technical package containing all resources needed to accurately calculate the SP-TAT-PH measure. This feedback was gathered via surveys and then further discussed by pilot participants during three collaborative webinars. Sufficient staffing enabled specialty pharmacies to take on new tasks (e.g.,

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DiversifyRx

JULY 11, 2024

Join our next Awesome Webinar Series with guest legal guru JD from Real Value Rx to answer any questions you have about the DSCSA delay. Small Dispensers and the 6/12/2024 FDA Announcement Concerning DSCSA This week’s article on the recent DSCSA postponement comes from PRS Pharmacy Services. The original article can be found HERE.

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DiversifyRx

NOVEMBER 30, 2023

Member-only perks such as free delivery or Rx packaging. Private webinars, FAQ sessions, or early access to programs for members only. Members should enjoy benefits that non-members don’t have access to, such as: Discounted prescription medications. Special pricing on over-the-counter (OTC) products.

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Viseven

AUGUST 15, 2024

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.

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ISPE

AUGUST 29, 2022

For changes requiring approval before implementation, once the necessary information has been submitted across regions, each health authority must review the data package and documentation based on local requirements. ISPE India Best Practices Webinars. Common Technical Document [CTD] sections). December 2020. 19 Cauchon, N.

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ISPE

JANUARY 10, 2023

The strategy is to provide an appropriate characterization package that demonstrates the alternative filter or resin will not impact product quality, submit it in a PAS, and, if needed, submit a request for an expedited review. US Food and Drug Administration webinar. Four proposed data packages and submission strategies follow.

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Pharmaceutical Technology

MARCH 22, 2023

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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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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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.

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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”.

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The Happy PharmD

FEBRUARY 28, 2025

Creating courses allowed me to package my knowledge into bite-sized lessons that not only educate but also generate income long after the initial effort. Webinar / Speaking Theres a unique energy that comes from speaking livewhether its at a webinar, conference, or workshop.

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