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Pharmaceutical packaging has come a long way in recent years. The industry constantly innovates to provide the most reliable and efficient packaging solutions, from automated assembly lines to shrink-wrap and other state-of-the-art technologies. Different types of pharma packaging include blister packs, bottles, and capsules.
Pharmaceutical packaging has come a long way in recent years. The industry constantly innovates to provide the most reliable and efficient packaging solutions, from automated assembly lines to shrink-wrap and other state-of-the-art technologies. Different types of pharma packaging include blister packs, bottles, and capsules.
The author highlights the importance of eco-friendly packaging, as green practices gain priority among consumers and companies globally. Eco-friendly packaging has become essential as green practices gain priority among consumers and companies globally. It’s not just about the individual, but also about the planet.
The rules were implemented to enhance patient safety protections via revised drug handling, packaging, and delivery requirements. The rules include changes to the notification process, medication packaging, the handling of reports, and safety issues. Hyman, Phelps & McNamara, P.Cs
FMCG Packaging Optimization in Seven Easy Steps Vijendra Fri, 05/24/2024 - 22:43 Packaging in the FMCG sector can account for up to 10% of input costs. Every percentage point saved on packaging costs can translate into substantial financial gains.
Product packaging has undergone major changes and now focuses on building sustainable capabilities to avoid dependence on eco-friendly materials. Meanwhile, companies are exploring eco-friendly solutions like energy-efficient refrigerants and sustainable packaging.
Discover How GEP Reduced a Retailer’s Packaging Costs by $25M annmarie@AZglo… Fri, 09/27/2024 - 23:24 Managing procurement can be a costly headache, especially when dealing with a fragmented supplier base and hundreds of redundant SKUs. A leading $16 billion U.S. supermarket chain faced exactly that — until GEP stepped in.
Some of our clients have successfully implemented strategies such as displaying supplier logos and QR codes on packaging, allowing consumers to easily access information about the ingredients and clinical results. Educating consumers about the value of branded ingredients is essential to further boost this trend.
CPG Firm Streamline Product Packaging and Improve Spend Control annmarie@AZglo… Tue, 06/27/2023 - 16:49 It may be challenging to predict demand and supply with absolute accuracy, but having advanced forecasting capabilities is crucial to effectively managing turbulent market conditions and supply risk.
In this blog , a summary of the key changes of relevance to primary packaging components and how West can help with the implementation will be discussed. Read more The post Are we set for the revised EU GMP Annex 1? appeared first on European Pharmaceutical Review.
In the case of parenteral drugs, CCI aims to avoid adulteration of the drugs packaged in vials, syringes, and cartridges. Even though these types of packaging systems are sealed in a hermetic manner, there are still many risks to mitigate. Vials, cartridges, and syringes are often packaged one of two ways. micron filter.
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 (..)
The company focuses on utilising packaging to minimise end-of-life waste and employs distribution methods that further reduce environmental impact. Downstream Activities (Scope 3) Lonza has designed optimised distribution networks to reduce transport distances to customers, ensuring efficient logistics with a lower carbon footprint.
Sustainable packaging for parenteral medicines Traditionally, the packaging of pharmaceutical products, especially in the parenteral medicine sector, has been resource intensive. The industry is transitioning towards materials that prioritize the planet – opting for biodegradable, recyclable, and smarter alternatives.
Driving environmental innovation: Green chemistry, waste management, and sustainable packaging in pharma In the quest for a greener future, pharma companies are embracing innovative strategies to minimise their environmental footprint. Furthermore, the development of eco-friendly packaging is gaining momentum.
FDA Law Blog readers receive a 10% discount off the tuition fee (promo code D10-999-FDA25 ). s John W.M. Claud will be speaking at the conference in a session titled “Crafting Your Safety Blueprint for Adverse Events and Recalls under MoCRA.” You can register for the conference here.
Key focus areas in sustainable manufacturing practices From drug discovery and manufacturing to packaging and patient engagement, sustainability should be embedded in every facet of pharma operations.
Therefore, in order to produce superior quality products, it is imperative to provide high-quality air, devoid of even the slightest trace of moisture for various stages of pharma processes entailing manufacturing, storage, research, testing, and packaging.
Effective January 3, 2023, BoardVitals is discontinuing its CME Pro Plus package. The post An Update on BoardVitals CME Pro Plus appeared first on BoardVitals Blog. This decision aligns with our core values, primarily trust and transparency with our customers. CME Pro Plus will simply no longer exist as an option for purchase.
Blogs – A company is free to own a blog or engage a blog writer by way of sponsorship or consultancy fees. In the EU and UK, where direct-to-consumer promotion of POMs is prohibited, companies may not sponsor blogs that promote, or could reasonably be expected to promote, such products.
There is hope that several of these proposals could be put into one larger health care package and passed during the lame duck session. Health Care Legislation There have been ongoing negotiations throughout the year about a slew of health care policy proposals.
eSTAR Templates As we have previously explained in our blog post here , eSTAR is an interactive PDF form designed to assist users in creating “complete” submissions. package labeling is optional). It includes questions about the product, that when answered, reveal additional information that should be supplied with a submission.
In July 2023, the House of Representatives’ Energy and Commerce Committee unanimously approved a package to reauthorize and strengthen the SUPPORT Act. Although the Energy and Commerce Committee’s package aims to strengthen the SUPPORT Act, some advocates believe more should be done.
They are continuing to invest heavily in the automation of manufacturing and packaging, improving productivity, operational cost efficiency, and labeling accuracy, proactively mitigating potential risks. The focus has shifted from manual and transactional processes to automation and strategic innovation.
Since it is likely this appropriations package will be one of the last meaningful pieces of legislation before the November elections, other policy priorities may be added to that final legislation as it gets closer to passage. We reiterated these priorities to start the year in January 2024.
Also, the packaging in which drugs and other medication are delivered to end-consumers is undergoing certain changes. Companies have also begun to commit to reducing their carbon footprint, increasing water neutrality and reducing waste created during and after the manufacturing process.
As part of these efforts, the government has implemented regulations mandating API (active pharmaceutical ingredient) manufacturers and pharma brands to incorporate barcoding on product packaging. This regulatory step is aimed at preventing falsified medicines from entering the market.
In this blog post, we will first briefly outline the procedural steps in the 510(k) review process for medical devices. However, the strategy of addressing the AI request presented in the next section of this blog post applies to all three types of 510(k)s. FDA Day (in calendar days) FDA Actions Day 1 FDA receives 510(k) submission.
Read this case study to learn how a global pharmaceutical leader fixed inefficiencies in a 25M packaging budget. How GEP Helped a Pharma Company Save $2M With Sustainable Sourcing priyanka.katke Thu, 01/16/2025 - 16:02 Balancing sustainability goals with cost efficiency in your supply chain management is no small feat.
In his remarks, Reiser discussed the current dynamics on the Hill and the possibility of an end-of-year health care package. Other Blogs: The Benefits of NHC Membership 07/25/2023 Read More Why is mental health awareness foundational for diverse communities?
Background FDA first introduced the final rule and guidance on eMDR in 2014 , which we blogged about here. For any major changes, additional time will be granted between the release of the implementation package and production deployment. User facilities are not required, but have been encouraged, to submit MDRs electronically.
In this blog post, we will explore best practices for pharmaceutical companies to navigate the complex landscape of regulatory challenges in marketing. Adhere to Labeling and Packaging Requirements The labeling and packaging of pharmaceutical products are tightly regulated to ensure safety and accurate information.
FDA intends the Guidance to provide “clarity and flexibility” to trading partners to “help ensure continued patient access to prescription drugs as the supply chain transitions to the interoperable, electronic product tracing at the package level under the DSCSA” while supporting “continued availability of products to patients.”
Before FDA even asked, we had been considering an HPM FDA Law Blog post on this subject. The appeal of distilling down the extensive process that goes into the decision to approve an application into a single package is easy to see, and some may be interested in only the ultimate distillation – an approval is issued or not.
As readers of our blog know, MoCRA was a significant change to regulation of cosmetics. Now in the second year of implementation, companies have started noticing the consequences as FDA implements the new requirements and develops regulations and guidance.
What assurance is there that counterfeiters who can easily mimic a brand’s packaging, name, and logo won’t also be able to mimic its QR codes? Google lens : Utilise the powerful visual recognition capabilities of Google Lens to capture and interpret codes on the packaging swiftly. System workflow 1.
All four manufacturers formulate and package finished pharmaceutical products (FPPs); none are limited to only packaging services, a sign of growing maturity. This post also appears on It's about Supplies , a blog from the the Reproductive Health Supplies Coalition (RHSC). kristine.gates… Wed, 03/13/2024 - 09:30 Global Health
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.
The long-awaited final rule, which we last discussed in a July 2023 blog post and have tracked in our March 2023 and March 2022 posts, aims to harmonize quality management system requirements for medical devices with requirements set forth by other regulatory authorities around the world. Notably, Part 820 will look different.
This R&D is not just for newer healing combinations, but also innovation across the product lifecycle (from formulation to disposal) for drugs that are less resource-intensive, increasing recyclability in packaging, and other environmental benefits like biodegradable formulations to reduce waste.
Other strategies can be waste minimisation, green packaging, energy efficiency and sustainable sourcing. On this World Environment Day, let us broaden our horizons to include the hidden yet pervasive issue of pharmaceutical pollution.
Food and Drug Administration (FDA) by API manufacturers to provide confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of human drug products. Read USP’s paper for strategies to enable geographic diversity of the medicines supply chain. _
In her recent Meet the Team blog, Advisory Council member Nicole Clausen shared great insights on how far veterinary inventory management has come since she joined the profession. You can read that blog here! You can read that blog here! How easy is it to order from them? Are there any barriers to the ordering process?
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