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Three industry bodies have produced a joint position paper highlighting recommendations for adopting a harmonised implementation of electronic Product Information (ePI) leaflets. It will also enable more patient-centric and accessible content by providing the most up-to-date information.
Common brand-name drugs that contain this ingredient include Ozempic , Wegovy , and Rybelsus all manufactured by Novo Nordisk, a Danish pharmaceuticalcompany. Youll know your semaglutide isnt compounded if you spot the brand name on the packaging and information leaflet. Compounded semaglutide can vary in appearance.
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.
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. Pharmaceuticalpackaging formats and materials. Pharmaceuticalpackaging formats and materials.
To cope with the growing demand for production flexibility and agility, IMA Group is structured according to highly specialised pharmaceutical divisions that concentrate on specific processing and packaging areas. Isolation technologies and other containment solutions are also part of our expertise.
On- or in-dose authentication means that a security measure or anticounterfeit feature is integrated with the dosage form itself, offering product verification and traceability embedded into each medicine, rather than on the secondary package” WHO estimates that >50 percent of the drugs for sale on the internet are fake.
By harnessing real-world evidence (RWE) and electronic health records (EHR), companies can make informed decisions. From eco-friendly packaging to socially responsible campaigns, sustainability resonates with today’s consumers. Data-Driven Decision Making Data is the lifeblood of effective pharma marketing.
Pharmaceuticalcompanies need to be prepared to answer the call for increased demand and supply into new markets, ensuring the proper resources and logistics framework are in place. While using high-capacity aircraft and minimal packaging reduces weight and increases capacity for vital products by using fewer flights.
The ERA therefore needs teeth – which does not mean it should be a barrier to the authorisation of new medicines – but it should require pharmaceuticalcompanies to minimise harmful effects on the environment, which indirectly also harm our health. Information on environmental effects of medicinal products. European Commission.
This could represent information specific to a particular patient, such as providing further information about their existing medical treatment, or it could involve a broader effort to educate the public on a specific issue. VR for real world education.
Within the EU, patient information leaflets (PILs) are not merely a regulatory requirement but a cornerstone of patient safety. These standardised documents provide meticulously curated and scientifically approved information. Exploring the benefits of ePI ePI offers advantages, notably swift access to updated medication information.
In this blog post, we will explore best practices for pharmaceuticalcompanies to navigate the complex landscape of regulatory challenges in marketing. Stay Informed and Updated Regulations in the pharmaceutical industry are constantly evolving. Keep thorough records of approvals for future reference.
With its highly educated, English-speaking workforce and high-quality medical facilities system, Singapore has attracted leading pharmaceuticalcompanies to open their regional headquarters in the city-state, including Novo Nordisk (Bagsvaerd, Denmark) and GSK. Additionally, Merck & Co.
Wholesalers can be either full-line wholesalers, who purchase the complete product line of a company, or specialised companies, which purchase speciality drugs to sell to clinics and hospitals. Selecting the best pharmaceutical wholesalers. GDP and GMP advisory. Temperature control facilities and supply solutions.
The company developing drug product through such an intense process, use to consider container closure system only for packaging of the product. [1] Thereafter, high quality standards were set for packaging and closure of such containers by the regulatory bodies. [2] Container Closure Integrity Testing Services Market.
In this blog post, we will explore best practices for pharmaceuticalcompanies to navigate the complex landscape of regulatory challenges in marketing. Stay Informed and Updated Regulations in the pharmaceutical industry are constantly evolving. Keep thorough records of approvals for future reference.
Applying what has been learned over the last three years to update pharmaceuticalcompanies’ approaches to development and implementation is key as the industry crafts its strategies in an increasingly digital and global environment. President, U.S. Business Unit and U.S. Country Head.
To combat such challenges, pharmaceuticalcompanies need to adopt processes that are not just efficient, but agile. Empowering labs with automated equipment that produces rich, traceable, and actionable data insights means pharmaceuticalcompanies can ensure drug production runs smoothly – even under stress.
Garabedian and his team plan to support VivoSense, not just with their funding package but with their industry network and connectivity. “We In 2010, when we founded VivoSense, we developed a software platform for analysis of wearable sensor data and electronic patient-recorded outcomes (PRO) and patient diary information.
Jouaville: A recent review, which evaluated the sampling methodologies used in RMM effectiveness studies , showed that a minority of these studies provided supporting evidence to inform the theoretical framework for the sampling methodology. She has worked with regulatory agencies and pharmaceuticalcompanies for over 10 years.
According to the GlobalData report Contract Injectable Packaging Trends in the Bio/Pharma Industry , more than half (55%) of FDA drug approvals in 2021 were accounted for by injectables. During the Covid-19 pandemic, large-scale vaccine production placed unprecedented demand on the parenteral packaging industry.
In an era where medicine is rapidly becoming more personalized, why do pharmaceuticalcompanies still struggle to effectively engage with the very individuals they aim to serve? Additionally, the COVID-19 pandemic has intensified public scrutiny of pharmaceuticalcompanies, creating a unique opportunity to build trust with patients.
The physicians provided their patients with cutting-edge therapies quite often found in the literature and not necessarily in the package insert. He also had the drug’s package insert. Unfortunately, both the vials and the package insert were written entirely in the “Swiss French” language. The hospital was ahead of its time.
Gathering consumption information. The lack of supply chain transparency The lack of supply chain visibility makes it excruciatingly challenging for pharma companies to plan medicine production, forecast demand, and manage their inventory. It also bears extra replacement expenses when drugs are discarded due to improper packaging.
As such there’s a growing question of how the industry will improve the sustainability profile of its existing medicines and ensure that sustainability is designed into new medicines, such as products, with a reduced environmental risk, greener manufacturing technologies, and recyclable delivery systems and packaging. 9 December 2021.
The Guidance applies to all member companies of EFPIA and IFPMA, but also acts as useful guidance for all pharmaceuticalcompanies as to how the authorities will interpret the legislative provisions to social media channels. The Guidance applies to both product-related and therapeutic-area-related activities.
Pharmaceuticalcompanies, regulatory agencies and governments are becoming increasingly concerned about fraud and counterfeiting throughout the pharmaceutical supply chain, especially with the cost of drugs going up. Europe is favouring 2D data matrix codes to encode information while the US is tending more towards RFID.
Contract marketing companies support pharmaceuticalcompanies in creating, improving, and maintaining their brand, as well as reducing risk, and ensuring better product placement in the market. Identifying the top commercial dose (non-sterile) companies in contract marketing.
It can also lead to difficulties in finding information, as it is often stored in disparate systems each with their own access rights and permissions.”. These are now used by several regulatory bodies, including the Food and Drug Administration (FDA) and the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) for submission packages.
Accordingly, pharmaceuticalcompanies are expected to up their investment in this area, both in terms of production infrastructure and expertise.”. For further information visit www.chiesi.com. Reducing the environmental impact of biopharmaceutical production is just one piece of the sustainability puzzle for the Chiesi Group.
Find the leading pharmaceutical solid dose manufacturing companies in contract marketing. Pharmaceutical Technology has listed the top solid dose manufacturing companies and solid dose pharmaceuticalcompanies based on our intel, insights and decades-long expertise in the sector.
Pharmaceuticalcompanies are accountable for ensuring that their medicine is safe when it comes into the hands of patients. Many countries have introduced serialisation legislation which requires product identifiers to be affixed to each package to provide traceability throughout the distribution supply chain.
Pharmaceutical compounding companies are expanding geographically and launching innovative products according to customer requirements to get a better foothold in the market. Active pharmaceutical ingredients (APIs). Packaging. • Benefits of pharmaceutical compounding. Excipients. Lab batch production. Formulation.
Additionally, the fill finish manufacturing of biologics is a critical step in the production of biopharmaceuticals as it requires well-equipped facilities with adequate sterile filling and packaging lines to ensure sterility of the product while filling into the final containers.
generic drugs at both small development companies and multinational pharmaceuticalcompanies. This unique pedigree gives the company a foundational understanding of how to launch products at every stage of development. Manufactured in the USA.
All traditional small molecule pharmaceuticals include carbon building blocks – by definition, organic materials – which are then transformed via modern synthetic chemistry to assemble the complex and highly variable skeletons that the final target structures demand. 9 In particular, the option of CCU is not widely considered.
In the 1990s, generic pharmaceuticalcompanies in the European Union (EU) offshored the manufacturing of active pharmaceutical ingredients (API) primarily to China. The European Commission plans to launch its revised EU pharmaceuticalpackage in Q1 2023 to ease drug shortages,” she says.
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.
When new information came up or there was a mistake, the current brochures had to be scrapped, and new ones had to be printed. While HCPs have the expertise to understand these concepts, they may find it overwhelming to synthesize, organize, and absorb all the information during short breaks between patients.
Hormone replacement therapy (HRT) explained (video) Evorel patches: out of stock update No specific information exists to why Evorel range went out of stock; however, last year there was a change of the ownership of Evorel range, which most likely contributed to delay in the manufacturing process. Evorel Conti patches are worn continuously.
“A lot of printed materials have been migrated to digital so that patients can opt-in to receive digital communications or HCPs can receive digital product or disease state information in the form of rep-triggered emails and microsites. The post What can pharma marketing learn from other regulated industries? appeared first on.
She attended several panels, listened to the conference speakers, and met a few professionals from different companies. “Omnichannel” is one of those new words many stakeholders at this summit heard of but still don’t exactly know what it means in terms of the transformation of healthcare and pharmaceuticals. .
Compared to other dosage forms, tablets are simpler to manufacture, package, and transport. As with any pharmaceutical manufacturing, challenges can be many, and processes are highly regulated.
In an era when the world is accelerating the development of drugs and targeted medicines using innovative technologies, pharmaceuticalcompanies still face registration hurdles for well-characterized molecules because of redundant or additional local regulatory requirements.
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