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2,3 Clinical implementation of CAR T-cell technology requires a reproducible T-cell manufacturing platform, which necessitates effective gene-transfer tools and T-cell culture conditions. Due to shipping and manufacturing requirements, the time from a patient being included in the CAR T programme to receiving therapy can be several weeks.
The use of vibrational spectroscopy, including raman mapping, to study pharmaceuticalproducts has been widely applied across the industry for several decades. These techniques can be utilised to understand polymorphs, intra- and inter-molecular interactions and solid form changes within pharmaceuticalproducts.
A market report has shown that to improve efficiency, quality and to reduce costs in drug manufacturing , Pharma has been adopting automated quality management systems, digitalisation of processes and integration of data analytics. What is limiting growth of the pharmaceutical quality management systems market? billion by 2031.
Understanding a product’s life cycle can assist a company in determining its position in the market relative to rivals and the success or failure of the product. Pharmaceutical packaging is strictly regulated and has to pay attention to ingredients, product quality, and adverse event labeling. Technology transfer.
Pharmaceutical supply chains are extremely vulnerable to the effects of climate change and face many challenges from sourcing to distribution. Reducing pharma's carbon footprint There are currently many initiatives aimed at reducing carbon emissions within the pharmaceutical industry.
In a recent video , pharmaceutical microbiology expert Tim Sandle highlighted areas of concern and attention relating to mycological contamination control in manufacturing. Pharmaceuticalproduct recalls due to fungal contamination have been increasing.
Prospects of the ampoules packaging market On the other hand, advancements in ampoule packaging, as well as sustainability measures and manufacturing innovations such as automation and robotics, were highlighted as promising contributing factors for growth of the market.
Processes in pharmaceuticalmanufacturing such as processing, milling, grinding, and mixing, are associated with the generation of dust. The researchers highlighted that the risks of hazard exposure include danger to the health of operators and cross-contaminations during manufacturing.
The CFU count distributions for bacteria and fungi presented a low and constant bioburden in the production environments, using both sampling methods. However, they noted that air and surface microbial levels “may vary” according to the sampling conditions and the pharmaceuticalproduction environments. 13 percent).
Pharmaceutical wholesalers act as intermediaries between pharmaceuticalmanufacturers and retailers and facilitate the delivery of the right medicines in a timely, efficient, and secure manner. Wholesale distributors are responsible for guaranteeing product quality and preventing the influx of counterfeited drugs.
To appreciate the scope of the challenge facing the pharmaceutical market, as well as patients across the globe, we must understand that there are two distinct threats – ‘counterfeit’ and ‘falsified’ medicines. There is also the challenge of falsified medicines – the fake, unauthorised medical products that make their way into the market.
In the pharmaceutical supply chain, blockchain technology has the potential to increase transparency and security, allowing for improved tracking and traceability of pharmaceuticalproducts. Blockchain technology is a distributed ledger system that enables secure and transparent transactions.
PharmaceuticalProduct Development (PPD). PPD, also known as PharmaceuticalProduct Development, is an extensive research organization headquartered in the United States but has a widespread global presence. Founded: 1985 Headquarters: Wilmington, North Carolina Annual Revenue: $65.0M Employee Size: 24,000.
Jiangsu Hengrui Medicine overview Jiangsu Hengrui Medicine (Jiangsu Hengrui) is a biopharmaceutical company that focuses on the research, development, manufacture, and distribution of novel pharmaceuticalproducts. Jiangsu Hengrui has R&D facilities in China, the US, and Japan.
Jiangsu Hengrui Medicine overview Jiangsu Hengrui Medicine (Jiangsu Hengrui) is a biopharmaceutical company that focuses on the research, development, manufacture, and distribution of novel pharmaceuticalproducts. Jiangsu Hengrui has R&D facilities in China, the US, and Japan.
Packaging plays a vital role in maintaining the quality, safety, user-friendliness and marketability of drugs and other pharmaceuticalproducts. The post Leading commercial packaging companies in contract marketing appeared first on Pharmaceutical Technology.
Product demonstration videos Medical devices and pharmaceuticalproducts might be complicated, thus it can be difficult to communicate their whole capability with conventional marketing tools. How Medical Video Production Benefits Healthcare Companies?
Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. What is the biggest impact of having compromised data when working with regulatory bodies in the pharmaceutical industry?
Johnson & Johnson overview Johnson & Johnson (J&J) researches, develops, manufactures, and sells pharmaceuticalproducts, medical devices, and consumer products. It is based on DuoBody technology platform. The drug candidate is a new molecular entity (NME).
Jiangsu Hengrui Medicine overview Jiangsu Hengrui Medicine (Jiangsu Hengrui) is a biopharmaceutical company that focuses on the research, development, manufacture, and distribution of novel pharmaceuticalproducts. Jiangsu Hengrui has R&D facilities in China, the US and Japan.
Shanghai Fosun Pharmaceutical (Group) is to collaborate with the International Finance Corporation (IFC) to construct a new pharmaceuticalproduction facility and distribution hub near Abidjan, Côte d’Ivoire. The IFC will provide two loans totalling $53.49m (€50m) to Fosun Pharma’s subsidiaries.
The number of unauthorised and unregulated online outlets selling counterfeit pharmaceuticalproducts is continuously growing, with many selling counterfeit medications via the internet typically posing as legitimate vendors. Covert-hologram seals are also atracting interest within the pharmaceutical packaging sector.
However, this greatly complicates both the worldwide distribution and stockpiling of vaccines and other drugs. This requires the development of technologies to rapidly produce effective, safe, stable vaccines that can be manufactured and distributed quickly. However, so far manufacturing has only been achieved on a modest scale.
The WHO called on key stakeholders, including regulators, governments and manufacturing facilities, to take immediate and coordinated action. In this instance of contaminated cough syrups, the concern is around an excipient in the product and not the active pharmaceutical ingredient (API).
Clearly the number one challenge in 2022, as mandated by the EU GMP Guidelines for the Manufacture of Sterile Medicinal Products Annex 1 1 , is the development of a Contamination Control Strategy (CCS),” Tony Cundell noted. He questioned how regulators will enforce revisions to Good Manufacturing Practice (GMP) regulations.
The pharmaceutical industry is one of the most heavily regulated sectors due to the direct impact of its products on public health and safety. Several factors contribute to the stringent regulatory environment: Patient Safety: Ensuring that the pharmaceuticalproducts are safe and effective is a crucial aspect.
Manufacturing delays and capacity issues that continue to impact the pharmaceutical supply chain have led to medicine shortages around the globe; an issue that has been exacerbated further by geopolitical events, the energy crisis and rising inflation. Globalisation and supply chain complexity are a factor.
In an age of disruption, technology is key to enabling pharmaceuticalmanufacturers monitor, track and control shipments and their processes. Pharmaceutical firms are changing the way they do business; the future winners will be highly automated and digitalised. But this results in huge, complex datasets.
In 2019, the pharmaceutical industry produced 48.55 As a critical industry, any disruption to the production or distribution of pharmaceuticalproducts can have significant cost implications for the industry and health ramifications for the global population”. Vulnerability .
The US Food and Drug Administration (FDA) has sent a warning letter to KVK-Techs drug manufacturing facility following an inspection in April 2019. The document identified significant violations of current good manufacturing practice (cGMP) regulations for finished pharmaceuticals.
Table of Contents: Understanding Pharma Tariffs Impacts on Branded Drug Marketing Adjusting Digital Advertising Strategies Strategic Recommendations for Pharma Marketers Conclusion FAQs Understanding Pharma Tariffs Pharma tariffs are taxes imposed by governments on imported pharmaceuticalproducts. FAQs What exactly are pharma tariffs?
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