Lisa W.’s Post

Over the past decade, the 7 best-selling #pharmaceutical #activeingredients in the European Union. Which ones made the list -- how much were the prices? In this age of cutthroat competition across the industry, prices matter greatly. #biopharma #pharma #trends #japanesemarket #biotech #europeanunion #fda #ingredients #blackfriday #pharmaceuticalindustry #thanksgiving #chemicals

Our PIREG-545 enhances quality control and compliance to industry standards. Read about how TOSS #HeatSealing components provide essential advantages for the #biotechnology and #pharmaceutical industries in Bio-IT World: bit.ly/3MYPIOq

Nitrosamine Impurities: One group of substances known to be very carcinogenic are nitrosamines. They can develop in drug substances and drug products via a variety of processes, most frequently involving secondary amines and nitrites. Because of the possible health concerns associated with nitrosamine impurities, the pharmaceutical industry has paid close attention to them, and regulatory bodies have placed stringent restrictions on their use in medication products. How it formed : Numerous processes can lead to the formation of nitrosamines, especially when secondary or tertiary amines and nitrosating agents (such as nitrites) are involved. These are a few typical routes: 1) Reaction Between Nitrites and Amines 2) Degradation Pathways a) Chemical degradation b) Physical degradation 3) Contaminated Raw Materials a) Raw material used b) Control Cross-contamination So this will be the topic of our discussion from now on. please suggest , if you required to add anything specific in this series. Pic Courtesy : https://lnkd.in/eHKbETrY

Standard methods of microbial contamination monitoring in the pharmaceutical industry are time consuming, outdated, and present a lot of risk when it comes to potential sources of contamination. Download this FREE case study to learn more about METTLER TOLEDO’s innovative solution to microbial contamination monitoring that improves process control, decreases risk of contamination, and gives accurate results in real-time. #7000rms #real-time #monitoring #pharma #mt #pro Download here: https://ow.ly/WBKg30sHXOL

Japan Aims to Cut Antibiotics Reliance on China by Resuming API Production https://lnkd.in/gFxbeMNu With government support, companies are reviving production of active pharmaceutical ingredients for antibiotics to protect a vital lifeline for public health. #economicsecurity #supplychain #pharmaceutical #antibiotics

With this solution, operators can effortlessly lift, split and empty sacks without losing suction. 👍 ✔️ Counterbalance base plate mounted ✔️ Lifting capacity – up to 100kg ✔️ Rotation 360 degrees It's ideal for production areas handling raw ingredients, such as food and pharmaceutical, as the contents can be emptied into a hopper seamlessly. Enquire about this product. ➡️ https://bit.ly/449oomX #FoodManufacturing #Pharmaceutical #VacuumLifting #MaterialHandling #Lifting #ManualHandling #HealthandSafety #LiftingEquipment

Dr. Reddy's is the earliest generic API manufacturer that has filed the US and Brazil DMFs for Tofacitinib citrate API and intends to file DMFs in all significant regulatory markets, ensuring comprehensive regulatory compliance and market entry. We offer crystalline polymorphic form and customized particle size distribution – D (0.9) < 60µ (un-micronized) - smaller particle sizes can be provided based on customer requirements. Our API's impurity profile strictly adheres to ICH Q3A guidelines. A comprehensive chemistry assessment has confirmed that the formation of GTI & nitrosamine impurities can be ruled out in its entire synthetic landscape. To learn more about our API offerings, download the tech sheet here: https://bit.ly/3k2evqe. #DrReddysXSustainability #GoodHealthCantWait #WeAreDrReddys #DrReddysAPI #ESG #Sustainability #APIPartner #Pharmaceutical #TofacitinibCitrateAPI #USDMF #BrazilDMF

💊“Consumers have long believed that more is better, that higher concentrations of active ingredients yield more powerful results. #Biotech dosages are more aligned with pharmaceutical standards than cosmetic standards. Take ibuprofen, for example. Too much ibuprofen is very, very bad for you, but very targeted, defined and scientifically proven amounts are very helpful. Likewise, in biotech, we optimize the dosage to keep it as low as possible, so you’re getting all the active ingredient benefits without unnecessarily exposing yourself to more activity.” 🍃Get the full story on where #natural #beauty ingredients and formulations are heading next: https://lnkd.in/gHQM-fCN

It gives us immense pleasure to share the April - June 2024 2nd quarterly issue of the "Excipience" newsletter which has insights from Pharmaceutical and Excipients Industry. This edition of the newsletter highlights the following: * Important News & Regulatory Updates * IPEC India in Media * IPEC India Annual Conference 2024 - A Report * Article on "Quick Look: The Role of Functional Excipients" * Article on "Keep Your Eye on the Supply" * Article on "JECFA reconfirms safe use of titanium dioxide in foods" Happy Reading !!! #newsletter #pharma #pharmaceutical #pharmaceuticals #excipients #excipient #ipec #india #magazine #articles #newsupdate #regulatory #regulatorycompliance #regulatoryaffairs #capsules #coprocessing #india #indianmarket #nitrosamine

Fill the blind spots in your cold chain. Learn more about how the implementation of compatible #sensor configurations and standardized #data-sharing processes can help improve visibility in the pharmaceutical cold chain. https://ow.ly/Kao250PlXGm #TeamGS1US