Global Pharma Tek Trading’s Post

Manufacturers of pharmaceutical products have long placed a high priority on maintaining the integrity of pharmaceutical packages. But over the last few decades, advancements in the health care field have also intensified problems with pharmaceutical packaging integrity. Testing the quality of the packaging for all healthcare products is crucial, but for parenteral drugs, the necessity is significantly increased. Even a minute breach in the package can cause microbial contamination leading to product deterioration. Hence ensuring container closure integrity is a critical process in the life cycle of parenteral products. Check out our video to know more. #microcurrenthvld #leaktestingparenteralproducts #containerclosureintegrity #parenteralproductsleakdetection #highvoltageleakdetection #ccit #ccitechnologies https://lnkd.in/dunFMv4w

Manufacturers of pharmaceutical products have long placed a high priority on maintaining the integrity of pharmaceutical packages. But over the last few decades, advancements in the health care field have also intensified problems with pharmaceutical packaging integrity. Testing the quality of the packaging for all healthcare products is crucial, but for parenteral drugs, the necessity is significantly increased. Even a minute breach in the package can cause microbial contamination leading to product deterioration. Hence ensuring container closure integrity is a critical process in the life cycle of parenteral products. Check out our video to know more. #microcurrenthvld #leaktestingparenteralproducts #containerclosureintegrity #parenteralproductsleakdetection #highvoltageleakdetection #ccit #ccitechnologies https://lnkd.in/dunFMv4w

Manufacturers of pharmaceutical products have long placed a high priority on maintaining the integrity of pharmaceutical packages. But over the last few decades, advancements in the health care field have also intensified problems with pharmaceutical packaging integrity. Testing the quality of the packaging for all healthcare products is crucial, but for parenteral drugs, the necessity is significantly increased. Even a minute breach in the package can cause microbial contamination leading to product deterioration. Hence ensuring container closure integrity is a critical process in the life cycle of parenteral products. Check out our video to know more. #microcurrenthvld #leaktestingparenteralproducts #containerclosureintegrity #parenteralproductsleakdetection #highvoltageleakdetection #ccit #ccitechnologies https://lnkd.in/dunFMv4w

Manufacturers of pharmaceutical products have long placed a high priority on maintaining the integrity of pharmaceutical packages. But over the last few decades, advancements in the health care field have also intensified problems with pharmaceutical packaging integrity. Testing the quality of the packaging for all healthcare products is crucial, but for parenteral drugs, the necessity is significantly increased. Even a minute breach in the package can cause microbial contamination leading to product deterioration. Hence ensuring container closure integrity is a critical process in the life cycle of parenteral products. Check out our video to know more. #microcurrenthvld #leaktestingparenteralproducts #containerclosureintegrity #parenteralproductsleakdetection #highvoltageleakdetection #ccit #ccitechnologies https://lnkd.in/dunFMv4w

🌡️🏭 Ensuring Precise Temperature Control in Pharmaceutical Warehouses 🌡️🏭 Did you know that maintaining the right temperature is crucial for storing pharmaceutical products? Most medications should not be stored above 25°C, making temperature control a top priority during the design phase. That's where Pharmaceutical Cooling Wholesalers come in! At EcoCooling, we take pride in our efficient and hygienic solutions. Our evaporative coolers use Electrically Commutated (EC) fans, the most efficient on the market. By operating at half speed, we can reduce fan energy use by over 85%. Additionally, our systems fully comply with legionella control regulations, ensuring hygienic operation through principles such as droplet avoidance and regular maintenance. For more information on possible installation techniques or to explore our innovative solutions, contact EcoCooling directly. Together, let's revolutionize pharmaceutical evaporative cooling and ensure the integrity of vital medications! 💊💙 #TemperatureControl #PharmaceuticalCooling #EcoCooling https://lnkd.in/exsbZS-Z

Effective Sterile Powder Transfer for Parenteral Drug Products 📣 Personalized medicine is an evolving field — offering targeted solutions that benefit patients by minimizing side effects and increasing effectiveness. This introduces a need for specialized fill-finish equipment that can efficiently route product into final packaging in an aseptic manner. Find out how a leading global contract development and manufacturing organization (CDMO), improved its powder transfer process for parenteral drug products without compromising efficiency or safety. Find this case study on our resource centre – https://lnkd.in/daT9bsK #PharmaManufacturing #CaseStudy #PersonalizedMedicine 

Are you sure your stopper is dry enough to be safe enough for your lyophilized drug product's stability? Have you ever experienced increase in residual moisture content in your lyophilized drug product and could not explain why? Do you know the moisture uptake capacities & water release characteristics of your lyo stopper? An increased residual moisture content could be caused by incomplete drying of the stopper after sterilization. Some stoppers feature a higher moisture uptake potential, weaker stopper drying kinetics and lower water release characteristics than others. Some stoppers are simply subjected to an inefficient drying process at the CMO – without anyone noticing. Check out our “check your lyo stopper“ service offering: You do not need to have a project running with us. You do not need to disclose your API nor any other details of your drug product. We simply need the sterilization and drying process protocol for your stoppers as performed at your CMO, and some stoppers (~ 100 pcs). Our experts will conduct a comparative evaluation on your stoppers versus modern state-of-the-art stoppers and carefully evaluate stopper drying kinetics, moisture uptake potential & water release characteristic. If you also want to find out whether you are already using a stopper that safeguards your lyo product, contact us at info@project-pharmaceutics.com. To learn more about our fields of expertise visit: https://lnkd.in/e_bPukQ3 #processdevelopment #lyophilization #freezedrying #pharmaceuticalmanufacturing #CRO

Are you sure your stopper is dry enough to be safe enough for your lyophilized drug product's stability? Have you ever experienced increase in residual moisture content in your lyophilized drug product and could not explain why? Do you know the moisture uptake capacities & water release characteristics of your lyo stopper? An increased residual moisture content could be caused by incomplete drying of the stopper after sterilization. Some stoppers feature a higher moisture uptake potential, weaker stopper drying kinetics and lower water release characteristics than others. Some stoppers are simply subjected to an inefficient drying process at the CMO – without anyone noticing. Check out our “check your lyo stopper“ service offering: You do not need to have a project running with us. You do not need to disclose your API nor any other details of your drug product. We simply need the sterilization and drying process protocol for your stoppers as performed at your CMO, and some stoppers (~ 100 pcs). Our experts will conduct a comparative evaluation on your stoppers versus modern state-of-the-art stoppers and carefully evaluate stopper drying kinetics, moisture uptake potential & water release characteristic. If you also want to find out whether you are already using a stopper that safeguards your lyo product, contact us at info@project-pharmaceutics.com. To learn more about our fields of expertise visit: https://lnkd.in/ePm5bWyF #processdevelopment #lyophilization #freezedrying #pharmaceuticalmanufacturing #CRO

📢 Exciting news! The EQUASHIELD® Syringe Unit has received FDA clearance for full-volume use. This milestone sets a new standard for safety and efficiency in the industry. When working with hazardous drugs, conventional syringes are limited to 3/4 of the volume, but with EQUASHIELD you can now utilize the full volume of each syringe with just 1 Syringe Unit! This means greater efficiency and cost-effectiveness in your drug handling practices. Experience the advantages of the EQUASHIELD® Syringe Unit's full-volume use: ✅ Cost Reduction ✅ Reduced Strain ✅ Time Savings ✅ Waste Reduction Read more here: https://hubs.ly/Q024gM390 At EQUASHIELD, your safety is our top priority. We're proud to provide a safer, more efficient, and cost-effective solution for your medication compounding needs. 💪💉 #healthcare #CSTD #chemotherapy #nursesafety #pharmacistsafety

LVP stands for Large Volume Parenterals, which are sterile solutions intended for intravenous administration in a volume of more than 100 mL. According to the International Council for Harmonisation (ICH) Q1F guidelines on Stability Testing of Pharmaceutical Products and the World Health Organization Technical Report Series (WHO-TRS) recommendations, the recommended storage conditions for LVPs are: Long-term storage: 25°C ± 2°C / 60% RH ± 5% RH or 30°C ± 2°C / 65% RH ± 5% RH.expand_more Accelerated storage: 40°C ± 2°C / 75% RH ± 5% RH. These conditions are based on climatic zones.exclamation Zone I/II countries, which have temperate climates, typically use 25°C/60% RH for long-term storage. Zone III/IV countries, which have hot and humid climates, typically use 30°C/65% RH for long-term storage. Here's a table summarizing the storage conditions: Storage Condition Tm (°C) RH (% RH) Zone Long-term 25 ± 2 60 ± 5 I/II Long-term 30 ± 2 65 ± 5 III/IV Accelerated 40 ± 2 75 ± 5 All It's important to note that these are just general recommendations. The specific storage conditions for a particular LVP will depend on the product itself and the results of stability testing. Manufacturers are required to conduct stability studies to determine the appropriate storage conditions for their products. These stability studies typically involve storing the LVP under a variety of conditions, including different temperatures and humidity levels, over a period of time. The product is then tested for its potency, sterility, and other important characteristics. The results of these studies are used to establish the shelf life of the product and the recommended storage conditions. #storage #stability #temperature #humidity #shelflife #qualityassurance