Remove Bioavailability Remove Containment Remove Packaging Remove Production
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EverGrain’s Line of Barley-Based Products Scores Upcycled Certification

XTalks

EverGrain Ingredients, a barley protein and fiber solutions company, recently received certification from the Upcycled Food Association (UFA) for its entire portfolio of products. The brand saw a unique opportunity to extract the excess barley to meet the global demand for sustainable, plant-based products. Barley Milk.

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The FDA’s Technical Rejection Criteria for Study Data: Does Your eCTD Submission Comply?

Camargo

A final binding guidance published April 2017, Providing Regulatory Submissions in Electronic Format — Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications required that electronic submissions be formatted according to eCTD submission standards and defined technical rejection criteria.

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Synthesis-to-Clinic®: integrating isotopic labeling and human ADME to reduce time to clinic

Pharmaceutical Technology

Study designs can be conventional, hybrid, or tracer studies, which can all generate the required data and be suitable to form part of the eventual regulatory submission data package. This has proved to be an extremely effective option for molecules where an understanding of absolute bioavailability is required.

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ProstaStream

The Pharma Data

Product Name: ProstaStream. If within the first 60 days of receipt you are not satisfied with Wake Up Lean , you can request a refund by sending an email to the address given inside the product and we will immediately refund your entire purchase price, with no questions asked. Description: Hello, my name is Frank Neal!

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Accurate dosing: How to achieve maximum precision with poor-flowing products

Pharmaceutical Technology

Due to rising healthcare spending, launch of novel treatments, and the rise of chronic diseases in an aging population, the global pharmaceutical packaging equipment market is rapidly expanding. But cost-effectiveness in drug-loading and production speed relies on dosing accuracy. Recent analysis valued the market [i] at USD 8.5

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Mitigating the risks of cross-contamination during Oral Solid Dose (OSD) manufacturing

Pharmaceutical Technology

There are a number of reasons why OSD forms dominate the market, not least because they are simple to administer, and it is easy to differentiate one OSD product from another. Compared to other dosage forms, tablets are simpler to manufacture, package, and transport.