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It is fair to say that patient-centred packaging is not mainstream for pharmaceutical packaging innovation and, furthermore, changing existing market‑approved packaging is unlikely to happen. 1 Regardless of how innovative a new drug is, it must be contained and packaged to deliver it safely to patients. Why is that so?
When launching a new product, revamping a marketing strategy, or aiming to build stronger customer loyalty, neuromarketing can help businesses: Understand consumer behavior on a deeper level Refine marketing strategies based on real, emotional responses Optimize product design and packaging to appeal to unconscious preferences Create campaigns that (..)
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.
Packaging plays a vital role in maintaining the quality, safety, user-friendliness and marketability of drugs and other pharmaceutical products. Finding the best commercial packaging suppliers in contract marketing. Pharmaceutical packaging formats and materials. Pharmaceutical packaging formats and materials.
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. Trends in clinical packaging.
Navigating the complexities of pharma and biotech packaging services can be difficult. With the growing number of complex therapies that require specialized packaging and handling requirements, selecting the right contract packaging organization (CPO) involves evaluating what services and additional benefits they can bring to your business.
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. Prefilled syringes offer a number of advantages over the more traditional glass vial.
By emphasising Accountability, Consistency, and Transparency (ACT) around manufacturing, energy and water use, packaging, and end-of-life, ACT makes it easy to choose more sustainable products.
Datwyler is a leading provider of parenteral packaging components and is helping the industry put quality first through the invention of the FirstLine® manufacturing standard. It also explores the causes of contamination and how parenteral packaging – one potential source – can be adapted to minimise the risk.
Your Agilent representative will work with you to create a customized package of services based on your lab’s technologies and application needs: Method maintenance Method implementation Method optimization Method development Support your entire pharma testing workflow with best-in-class analysis solutions from a trusted source.
The company has already formed partnerships with other third-party software developers to extend the functions of cobas pulse, which are already bundled with the unit, ready for download, or will be available soon.
While using high-capacity aircraft and minimal packaging reduces weight and increases capacity for vital products by using fewer flights. To learn more about how Tanner is adapting to changes in the clinical trial supply chain and embracing technological innovations, download this white paper. Download to learn more.
Download the Research Guide Research Guide Key Dates August – Submissions Open Early December – Excellence Award winners announced Benefits for Winning Companies Independent recognition solidifies your business as a trustworthy brand. Frequently-Asked-Questions (FAQ) Are there any costs involved in the awards?
ISMP encourages organizations to maintain, update, and periodically review a list of oral dosage forms that may require alteration through evaluation of package inserts, drug manufacturer inquiries, tertiary drug information resources, and primary literature.
In this one-pager, which you can download below, you will find an overview of techniques as well as an explanation of which ones can be used for specific tasks (from sample identification to packaging and tableting).
Addressing labelling and secondary packaging challenges in the early stages BAP Pharma specialises in clinical trials supply, with expertise in comparator sourcing, secondary packaging, distribution, and medicines access. Upcoming biotechs need to get moving and they don’t have time to wait for a packaging slot for eight months.
A new case study from GEP details how a global consumer packaged goods manufacturer transformed its source-to-pay processes to improve focus on indirect spend and deliver significant savings.
Primary Packaging Development. Delve into the considerations for material components for the development of primary packaging. Kevin Kusmierek, Scientist, Primary Packaging and Medical Devices, CSL Behring. Michael Becker, Packaging Engineer, Boehringer Ingelheim. Sustainability for Injectable Delivery Devices.
For the FREE basic package , there is a limit of 2 wists, maximum of 1800 data rows and 1 GB monthly user downloads. You have to first save your spreadsheet file as CSV UTF-8 format in Microsoft Excel , instead of drag in your normal Excel file. Also, 1 GB of space is provided for file manager feature with 10 GB bandwidth per month.
Quality in terms of number of defective items, packaging and labelling, quality management system certification, research, development, and innovation. . · Temperature control facilities and supply solutions. Worldwide sourcing and drop-ship of orphan medicines, and. Warehousing and logistics services.
It is critical to understand the supply chain, plan your packaging, storage and distribution lanes, then test the entire process before patient shipments go live. Products are stored and packaged in a dedicated suite by a dedicated team,” explains MacNeir. The requirements When handling personalised medicines, time is of the essence.
The QR code, which appears on its consumer-facing packages (usually a blister pack), contains a serial number thereby conferring a unique digital identity to each package. A table with the results of my analysis can be downloaded from an online portal [4]. I expected to see something similar in the Levipil case.
The webinar also highlighted advanced analytical techniques for detecting PFAS in food matrices, including seafood, eggs, meat, infant formula, and packaging materials. Global and regional regulations are discussed, with a focus on evolving standards in India and the South Asia Pacific region.
We’d like to get to a point where our treatment and prevention offering can be packaged together for the NHS – because both go hand in hand, alongside digital tools”. We’d like to get to a point where our treatment and prevention offering can be packaged together – because both go hand in hand, alongside digital tools.”.
Container Closure Integrity Testing (CCIT) is used to evaluate the ability of a pharmaceutical’s primary packaging to protect the sterility of its contents. On a regular basis, pharmaceutical manufacturers are performing CCIT during commercial production to ensure that packaging processes are operating as they should.
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.
The companies offer various solid dose products and services including, but not limited to, formulation and analytical development, manufacturing capabilities, technology transfer and scale-up, quality and regulatory support, commercial manufacturing, packaging, and warehousing.
While Catalent Inc and PCI Pharma Services are in charge of the solid dose and packaging of Lupkynis, Lonza is manufacturing the small molecule API. Vetter Pharma-Fertigung GmbH & Co KG is conducting the parenteral manufacture and packaging for Trulicity. Please check your email to download the Report. By GlobalData.
billion in 2020 (Packaged Facts) Pet medication sales have grown at a healthy CAGR of 9% since 2017 (Packaged Facts) Veterinary practices are unique in that they can sell medications directly to their clients, which provides an important revenue stream for the business. Download Your Copy 3. Bn in 2020 to over US$ 2.7
Compared to other dosage forms, tablets are simpler to manufacture, package, and transport. Download the whitepaper below to find out more about ILC Dover’s flexible solutions for protecting the entire supply chain. Please check your email to download the Webinar.
The information contained within the download document is intended for pharmaceutical manufacturers, wholesalers, retailers and distributors, pharmaceutical executives, medical representatives, business development managers, retail salesmen, sales managers, pharmacy executives, and any other individual involved in pharmaceutical marketing.
Quotient Sciences supported a standalone DCS classification and formulation development package. Please check your email to download the Whitepaper. A recent example of this was for a compound at the candidate selection stage. Grass and P. S54 – S61 (2001).
We source as much of the materials as we possibly can locally, even packaging,” he notes. When we need new packaging, it is really simple to get and it is quick. To learn more about the development and partnership opportunities for businesses within Scotland’s health sector, download the document on this page. Free Whitepaper.
Finally, one of the most important attributes of an advanced CCIT method is high sensitivity: can it detect packaging defects as small as 1 micron to provide ultimate assurance of product sterility? Please check your email to download the Whitepaper. Traditional, probabilistic CCIT methods fail to meet many of these criteria.
Packaging needs?. Important items to look out for in the proposal include information on what was requested in terms of batch size, number of batches expected per year, component confirmation, and the packaging plan.???. Drawings and/or part numbers of the selected container closure? Reviewing proposals???.
The preparation of a semi-solid dosage form – from formulation and development, to scale-up, commercial manufacturing, and packaging – should ideally take place under one roof in a contiguous, end-to-end workflow to avoid unnecessary equipment and process changes. To find out more, download the whitepaper below. Free Whitepaper.
ISMP encourages organizations to maintain, update, and periodically review a list of oral dosage forms that may require alteration through evaluation of package inserts, drug manufacturer inquiries, tertiary drug information resources, and primary literature.
Packaging. • The information contained within the download document is intended for pharmacists, pharmaceutical executives, sales managers, manufacturers, business development managers, pharmaceutical sales representatives, and any other individual involved in the pharmaceutical compounding sector. Excipients. Lab batch production.
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