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Johnson & Johnson is recalling sunscreens from two of its popular brands over concerns of carcinogenic benzene contamination. The company said that while benzene is not an ingredient in any of its sunscreen products, it was detected during routine internal testing in some samples of its aerosol sunscreen finished products.
In this article, Ben Hargreaves asks whether there is particular potential for the technologies to revolutionise staff training and reduce costs in pharmamanufacturing. The pharma industry’s overall push into industry 4.0 The importance of manufacturing. which is critical to Pharma 4.0,
When freeze drying sterile pharmaceuticals, mass spectrometry helps manufacturers protect valuable batches from silicone oil contamination – a possible risk of the lyophilisation process. Preventing silicone oil contamination Silicone oil is a common component of lyophilisation systems.
This, coupled with small pharmacompanies being unable to acquire or access containment capabilities in-house, means that the demand for innovative specialized small molecule capabilities remains high. Of those, only 935 (34%) small molecule API facilities offered some type of containment capabilities.
Manufacturers are actively looking at ways they can improve drug delivery through well-designed parenteral packaging systems, and the choice to deploy prefilled syringes for more and more injectable drug products is a key part of this push. Cost is an important final factor, especially for small and mid-sized pharmacompanies.
Despite the current emphasis on biologic medicines, small molecule drugs still dominate the pharmaceutical manufacturing world. Manufacturing these highly potent and often cytotoxic drugs introduces many risks for operators and the environment. Cross-contamination of standard products with highly potent ones is another key concern.
The first lawsuit claiming that gastrointestinal drug Zantac causes cancer has been voluntarily dismissed a week before it was due to come to trial, in an early victory for the pharmacompanies that will defend themselves from the allegations. “GSK will continue to vigorously defend itself against all claims alleging otherwise.”
At Creogenic Pharma, we have a dedicated workforce of professionals and a cGMP compliant manufacturing facility. We also have contamination-free spacious warehouses and link-ups with certified vendors in the industry. SEND ENQUIRY [contact-form-7] The post Best Cough Syrups in India appeared first on Creogenic Pharma.
From discovery to development and production of any biological product, aid in decision making is given by Pharma Consultants. A group of experts specialized in the field of pharmacology deals with clinical/non-clinical testing, biologic design and manufacturing, regulatory agency interactions, submission preparation, and so on.
Yet while demand for injectables soars, regulators are cracking down on quality requirements, forcing many pharmacompanies to examine the role – and risks – of their primary packaging. The need for quality When it comes to injectable medicine, achieving product sterility through aseptic manufacturing is of critical importance.
Regulatory decisions have a ripple effect, first affecting the pharma sponsors, and then the companies tasked to manufacture the drug. Pharmaceutical Technology looks at drugs and biologics with recent regulatory verdicts that will likely impact manufacturing volumes. Consequential FDA and EMA decisions.
The top ten pharmacompanies in 2023 by revenue accounted for about 35 percent of the market value, with total earnings of $559.5 The top big pharma players have remained relatively consistent in their market positions over the past several years. Here is a look at the top ten pharmacompanies in 2024 based on 2023 revenue.
Water-borne illnesses are also likely to become more common, as increased rain and storm surges contribute to flooding and contaminated run off. Just as in the wake of COVID-19, the world will look to pharma to fulfil its public health needs. Vulnerability . Making plans is not enough.
While RT-PCR methods can handle some level of multiplexing, they do require specialized, contamination-free environments. Rapid assays that can deliver same-day results are highly attractive to pharmacompanies, as they eliminate lengthy sample queues often seen with centralized or outsourced testing.
Medical device manufacturers are leveraging these technologies to enhance their products, supporting healthcare providers and improving patient outcomes. This reduces human error and contamination risks, ensuring higher-quality production outcomes. The global next-generation biomanufacturing market is projected to grow at a CAGR of 14.85
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