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By Christopher Weikart, Chief Scientist at SiO2 Materials Science Why is an incredibly innovative and forward-thinking industry like pharmaceuticals being held back by the products that haven’t changed in over a century?
Packaging plays a critical part in the pharmaceuticals and medical devices industries and is developed with its own set of security standards for the safety of consumers. The role of primary packaging has extended beyond the primary objectives of sterility, physical and chemical protection, and security.
Food processing and packaging solutions company Tetra Pak is partnering with synchrotron radiation laboratory MAX IV to launch the next generation of food packaging: fiber based packaging. Using renewable materials and increasing the use of fiber-based material within packages will be vital.
Clinical packaging and labelling follow stringently controlled procedures and high-standard quality control measures to assure the safety and functionality of investigational medicinal products, during their storage, distribution, and use. Finding the best clinical trial packaging services providers.
A container closure system consists of all the packaging components that contain and protect a pharmaceutical product. A container closure system protects the product from environmental conditions, safeguarding a product’s purity, strength, safety and efficacy. Container Closure Systems. extractables and leachables).
Behind the scenes, generic drug manufacturers are working tirelessly to ensure that their products are safe, effective, and identical to their branded counterparts. It helps them to identify potential issues early on, make adjustments as needed, and ultimately bring a high-quality product to market.
— Scientists working to understand the cellular processes linking high cholesterol to breast cancer recurrence and metastasis report that a byproduct of cholesterol metabolism causes some cells to send out cancer-promoting signals to other cells. These signals are packaged in membrane-bound compartments called extracellular vesicles.
Formulating products that have the proper composition, viscosity, texture, and stability, and can also be shown to be safe and effective, is both a science and an art. Without proper precautions, knowledge gaps can occur and important details may be overlooked when a product is transferred from one site to another. Simplicity matters.
As regulatory requirements become increasingly harmonized across the globe, the development and marketing of pharmaceutical products worldwide are also becoming more streamlined. The decentralized procedure applies to all products without a prior marketing authorization in the EU that are not required to use the centralized procedure.
MIT engineers have designed a food sensor , made from an array of silk microneedles, that can pierce through the plastic packaging of foods to sample for bacterial contamination and spoilage. The Velco-like device pierces the packaging and the food via silk microneedles that suck in material through capillary action.
It created the possibility of more easily obtaining information to support new product indications or to help with post-approval study requirements. In October, the FDA took a step towards clarifying these questions with a guidance called “ Data Standards for Drug and Biological Product Submissions Containing Real-World Data.”.
Phthalates are commonly used to make products—including artificial leather, footwear, plastic food packaging, and personal care products—more flexible or stable. However, scientists do not completely understand if or how it harms the human body. To do so, researchers looked at the effect of […].
Saliva production is primarily driven by mechanical and gustatory (taste) stimulation (Dodds et al., In today’s post, I will review the best dry mouth lozenges for saliva production. I will also list products which can be may be available to buy from the pharmacy. Alternatives products to manage dry mouth.
Scientists from the University of Plymouth and University of Illinois at Urbana-Champaign tested a range of new and used products including children’s toys, office equipment […].
The expanded use of the INitial Targeted Engagement for Regulatory Advice on CBER/CDER ProducTs (INTERACT) meeting : INTERACT meetings are intended to facilitate IND-enabling efforts where a sponsor is facing a novel, challenging issue that might delay the progress of the product towards entry into the clinic in the absence of this early FDA input.
These companies often have limited in-house resources for product development or scale-up, and so depend on CDMO partnerships to achieve development milestones. Narrower Product Focus Emphasis on Development End-to-End Support and Manufacturing Flexibility Manufactured in the USA Continuous Reinvestment. Narrower product focus.
As the new law unfolds—and as state laws regarding ingredients and packaging, as well as laws regarding environmental claims continue to affect the cosmetics and personal care industries—the topics covered at the conference have never been more relevant. By John W.M.
Biodegradable packaging and products are seen by many as part of the solution to the global plastics crisis. To address that, a team of UK scientists has been awarded £2.6million for a four-year project assessing how […].
The list includes providers of development services, biologics management supply chain solutions, clinical trial services, commercial and logistics services, as well as packaging, labelling and distributing services for biologics.
Streamlined development, flexibility in manufacturing, and improved product quality at reduced costs, while gaining access to capabilities and capacity are some of the factors fuelling the pharmaceutical solid dosage contract manufacturing market. Find the leading pharmaceutical solid dose manufacturing companies in contract marketing.
In many cases, pharma companies select a contract development and manufacturing organisation (CDMO) to develop products versus doing the work themselves for reasons related to cost, convenience, and capacity. In nearly all cases, developing a PDF from an ADF requires additional product development work.
In recent months, the Federal Courts have twice upheld Health Canada’s findings as to what is, and is not, a natural health product. The Courts’ decisions provide insight into how natural health products are distinguished, under federal law, from cosmetics and from drugs subject to the Food and Drug Regulations.
Primary Packaging Development. Explore updates to drug device combination product design approaches considering patient preference at the forefront with case studies from big pharma representatives. Delve into the considerations for material components for the development of primary packaging. Connected Drug Delivery Devices.
Medical imaging tech company Polarean Imaging has recently announced that the US Food and Drug Administration (FDA) has approved their drug-device combination product Xenoview (xenon Xe 129 hyerpolarized). After hyperpolarization, it is packaged into a dosage delivery bag.
“The healthcare industry has one of the heaviest environmental footprints, and manufacturers are increasingly faced with regulations to make more sustainable products,” said Mohammad H. Behfar, senior scientist at VTT, in the news release. Bio-based substrates like cellulose e-skin are promising alternatives to fossil-based ones.
Scientists in Spain and the US are pioneering these alternatives to chemical preservatives in meat, which could revolutionize how the meat industry extends meat shelf life and ensures food safety. The team wonders how these nitrite alternatives could impact the taste of meat but commends these scientists for studying substitutes.
Quotient Sciences helps biotech and pharma customers in the development and optimization of drug products. Our chemists and formulation scientists review the properties of new drug candidates and “work their magic” to develop formulations that improve the exposure profile of the compound.
This product was developed by uniQure prior to being licensed to CSL Behring. In simple terms from a non-scientist, these gene therapies add functional versions of genes to patients that do not have them, and thus the idea is to have these genes function in the same way as they do in individuals without these disorders.
Scientists used synthetic biology and computational protein design tools to develop an enzymatic process to transform red cabbage anthocyanins into their desired color. This process has been used in the food industry before, such as in cheese production, for example. These labels must be present on the packaging of the items sold.
Preservatives and additives serve as routine ingredients for manufacturers, extending the shelf-life of food products. Related: Scientists Urge the FDA to Ban Red 3 Color Additive 1. Unfortunately, these dyes are often in food products intended for infants and young children, but no precautionary labeling is mandated domestically.
Heather Barnes, external innovation lead EMEA at Johnson and Johnson Consumer Health, is a scientist who is truly passionate about consumer health. I am fascinated by the breadth of my role, which encompasses self-care products, skin health, sustainability and much more. From the very beginning, I thought, ‘Right, I love this!
GSKCH, which is due to separate into a new company next year, has found an innovative way to leverage renewable raw materials for high-performance oral care products – helping reduce the use of fossil fuels for virgin plastic. It is a byproduct of paper production, and would otherwise be disposed of.
State-of-the-art cryogenic freezers alongside material transfer equipment have been installed that are designed to retain the integrity of investigational advanced therapy products by minimizing their time-out-of-environment. Catalent helps accelerate over 1,000 partner programs and launch over 150 new products every year.
The objective of most trials is secure product approval, indication approval or assess the long term safety of the product after it is approved. Unfortunately, the FedEx package drop-off time is 4:00 pm and the pick-up truck has left for the day. A great project manager would drive to the airport and drop off that package.
The Future of Drug Delivery and Combination Product Device Design. The pre-filled syringes industry is growing at an exponential rate with innovations in parenteral delivery device development to aid self-administration and deliver biologics, high concentration, and large-volume drug products. BOOK BY 29 TH OCTOBER AND SAVE £200.
Some scientists , however, say there are not enough studies supporting the marketing claims made by ionized water companies and others believe the claims are nonsensical. Tackling plastic waste is also a part of Nestlé’s goals, calling it a major threat to our planet and aiming to develop the most sustainable packaging for its products.
“They came up with ways to package the ingredients to resemble the fatty, juicy mouthfeel of a real chicken tender.” “Our scientists have a very good understanding of animal product at the molecular level. But also, the product that we have, we understand the gap between the two.
To develop REGN-COV2, Regeneron scientists evaluated thousands of fully-human antibodies produced by the company’s VelocImmune ® mice, which have been genetically modified to have a human immune system, as well as antibodies identified from humans who have recovered from COVID-19.
MDC, the independent national centre for innovation in drug discovery, has a major focus in pre-clinical imaging and will now offer the design and production of radiotracers alongside its cutting-edge imaging and industrial drug discovery expertise based at nearby Alderley Park.
Large equipment, including centrifuges, imaging systems and fume hoods, are shared among all lab members, and are usually located between individual workspaces, meaning that a scientist will have to cross over their colleagues’ workspaces multiple times during the course of a single experiment.
To develop this novel medicine, Regeneron scientists evaluated thousands of fully-human antibodies produced by the company’s VelocImmune ® mice, which have been genetically modified to have a human immune system, as well as antibodies identified from humans who have recovered from COVID-19.
A deep dive into the list reveals that the formula for a high level of employee satisfaction is a mix of competitive financial packages, benefits such as healthcare, education support and professional development, wellness initiatives, recognitions for achievements and diversity and inclusion.
As we prepare to provide these first doses, we will provide support so that countries can ensure that solid systems are in place for vaccine delivery, building on our recent innovations in packaging to manage cold chain requirements.
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