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government on Thursday unveiled an $800 million package to bolster the life sciences, highlighting officials’ efforts to grow the industry even as biopharma companies have raised alarms about policies they say are deterring them from investing further in the country. LONDON — The U.K.
This poses a significant challenge for pharmaceuticalmanufacturers, not least because of the technical challenges related to operations, supply chain and the environment. This article explores the potential impact of the proposal and considers how manufacturers can ensure the safety and reliability of their products.
Bringing together over 225+ exhibitors and showcasing 12000+ products and solutions, the expo will represent diverse industries, including pharmaceuticalmanufacturing, biotechnology, medical devices and diagnostics, cosmeceuticals, nutraceuticals, packaging solutions, and healthcare IT.
PharmaceuticalManufacturing & Packaging Congress (PHARMAP 2022) covers the current state of the pharmaceuticalmanufacturing and packaging industry. The Congress gathers pharmaceutical companies, CMOs and CDMOs, governmental bodies together with pharmaceutical equipment providers and service companies.
According to the European Federation of Pharmaceutical Industries and Associations (EFPIA), more than 600 essential medicines are at risk if a proposed restriction on the use of fluorinated substances, per- and polyfluoroalkyl substances (PFAS) across pharmaceuticalmanufacturing in the EEA, is implemented.
PharmaceuticalManufacturing & Packaging Congress (PHARMAP 2021) will be held on the 28th – 29th of June, 2021 at the BGS online platform. PharmaceuticalManufacturing & Packaging Congress provides the networking platform for the decision-makers from the pharmaceutical industry.
PharmaceuticalManufacturing & Packaging Congress (PHARMAP 2022) is held on June, 20-21, 2022 in Berlin, Germany. PharmaceuticalManufacturing & Packaging Congress provides a networking platform for decision-makers from the pharmaceutical industry to share cases and brand-new solutions in one place.
Blow-fill-seal (BFS) technology has long been a cornerstone of pharmaceuticalmanufacturing, relied on for packaging sterile liquid medications, including but not limited to ophthalmic and respiratory drug products.
Revolutionising pharma the adaptive way Pharmaceuticalmanufacturing is undergoing a transformative development, driven by innovative technologies that enable right-first time (RFT) production and adaptive scaling to meet changing demands. Why is adaptive manufacturing necessary?
Pharma Tech Industries, a pharmaceuticalmanufacturing and packaging solutions contractor for wellness products and medical devices, has announced the appointment of their new chief executive officer Darrin T Schellin.
Leaders of the whole pharma value chain meet at PharmaceuticalManufacturing and Packaging Congress (PHARMAP) to find new connections and discuss trends of the industry.
The first day of the Congress started with the executive opening panel, where speakers from LabWare, Optel Group, 3V Tech, GSK, PharmaLedger Association, Bushu Pharmaceuticals, PHARMAZAC had a discussion about new models for pharma manufacturing and packaging.
The market for pharmaceuticalpackaging will grow by 8.24 per cent worldwide and the market for pharmaceuticalpackaging machines by 7.5 Steriline will showcase a Robotic Vial Filling Machine (RVFM5) that merges these qualities for the primary packaging of injectable drugs. per cent per year until 2028 1.
The company focuses on utilising packaging to minimise end-of-life waste and employs distribution methods that further reduce environmental impact. As Lonza demonstrates, sustainable practices are not just environmental imperatives but essential components of modern pharmaceuticalmanufacturing.
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.
Novo Nordisk has announced plans to invest over 42 billion Danish kroner (nearly £5 billion) starting in 2023, to expand its manufacturing facilities in Kalundborg, Denmark. According to the pharma company , the financing will add to global capacity: from manufacturing of active pharmaceutical ingredients (API) through to packaging.
Indeed, a key aspect of EU GMP Annex 1 is the requirement for pharmaceuticalmanufacturers to develop a comprehensive Contamination Control Strategy (CCS) that documents their approach to assuring the sterile drug product’s high quality and, therefore, enhancing patient safety.
Warning letters issued by FDA can be an important source of data to study and analyse violations that occur in pharmaceuticalmanufacturing. Such studies can also help companies prepare for their upcoming inspections by enabling them to identify and rectify any issues.
43: Identification and Classification of Nonconformities in Moulded and Tubular Glass Containers for PharmaceuticalManufacturing. Specifically, the document covers the development process of glass containers for pharmaceutical products, glass container sampling as well as definition of lots.
Curious about sustainability in pharmaceuticalmanufacturing and the supply chain? EPR Podcast 22 – Pharmaceuticalpackaging – Manu Kittanakere, Gilead The post Joint investment to accelerate UK sustainable biomanufacturing appeared first on European Pharmaceutical Review.
Consequently, pharmaceuticalmanufacturers risk their reputation if impersonating products fail to deliver the expected quality or health impact. These may be mislabelled or produced in fake packaging and, most dangerously, there is no regulation around their manufacture. But what exactly does this look like? .
Enhancing talent in pharmaceuticalmanufacturing “Talent and skills are fundamental to successful innovation and industry growth. This newly announced grant is part of the £650 million ‘Life Sci for Growth’ funding package launched in May 2023.
Contract research, development and manufacturing organisation (CRDMO) WuXi STA has broken ground on its new 190-acre pharmaceuticalmanufacturing campus in Middletown, Delaware, US. The biopharmaceutical industry is part of Delaware’s DNA,” stated Delaware Governor John Carney.
However, with cleanrooms-on-demand representing a feasible and accessible opportunity for those across pharmaceuticalmanufacturing, what are the key challenges in adoption and how can we expect the industry to overcome them to reap the rewards on offer? But with a single dedicated cleanroom environment costing around $2.5
Nexus Pharmaceuticals President and CEO Usman Ahmed said: “We are thrilled to receive the EIR for our Pleasant Prairie facility. This is a major milestone for our company and reflects our commitments to reshoring sterile pharmaceuticalmanufacturing to the US.
IPA also addressed concerns regarding transparency in drug manufacturing locations. It noted that US law requires complete manufacturing addresses to be printed on generic drug packaging and listed in the FDAs Orange Book database.
Recent European manufacturing investments Earlier this month, Novo Nordisk announced that it was planning another manufacturing facility expansion, this time at its site in Kalundborg, Denmark. In September, the Novo Nordisk Foundation announced a multi-million financial commitment to another Denmark-based manufacturing facility.
It provides an unparalleled platform for stakeholders to participate in extensive dialogues covering pharma machinery, packaging, analytical instruments, laboratory technologies, equipment, ancillaries, ingredients, and beyond. billion (Rs 2.1 lakh crores) in the 2022–2023 fiscal year.
Implementing PAT in (bio)pharmaceuticalmanufacturing New sensors or larger equipment with more complex setups (software and hardware) require stringent procedures to become fully implemented in a good manufacturing practice (GMP) manufacturing facility.
Whereas proper disposal of unused medications, as well as initiatives to reduce packaging waste, chemical waste, and improve recycling programmes, will aid in pro-actively addressing this challenge. This may involve the use of eco-friendly raw materials, green manufacturing processes, and eco-friendly packaging.
On October 6, 2024, the Federation of Pharma Entrepreneurs (FOPE) and PharmaState Academy conducted Session 6 of the PULSE (Pharma Upgradation & Learning Series for Excellence) initiative, focusing on HVAC Systems and Qualification in pharmaceuticalmanufacturing. The session began with a keynote address by Thiru M.
What are the top 3 trends that defined pharma manufacturing in India and globally in 2024? In 2024, the pharmaceuticalmanufacturing landscape underwent transformative changes, driven by technological innovations, regulatory adaptations, and evolving global demands. Regulatory bodies in the U.S.
In frames of PHARMAP 2023 speakers are going to talk about the sustainable future of the pharma packaging model and present topics regarding recycle-able vs biodegradable solutions in pharma packaging and packaging solutions for security and brand protection.
The Food and Drug Administration (FDA) has successfully inspected Nexus Pharmaceuticals’ pharmaceuticalmanufacturing facility located in Pleasant Prairie, Wisconsin, US. The inspection will allow the company to commence commercial operations at the three-storey, 84,000ft² manufacturing facility.
Pharmaceutical wholesalers act as intermediaries between pharmaceuticalmanufacturers and retailers and facilitate the delivery of the right medicines in a timely, efficient, and secure manner. The post Leading pharmaceutical wholesalers appeared first on Pharmaceutical Technology.
They comprise interconnected webs of local and global ingredient suppliers, manufacturers, packagers, distributors, providers, and regulators. active ingredients, excipients, other raw materials) Packaging materials (e.g., Global supply chains are complex and vulnerable to disruption.
211.130 Packaging and labeling operations quotes, – There shall be written procedures designed to ensure that correct labels, labeling, and packaging materials are used for drug products; such written procedures shall be followed. Different products should not be packaged in proximity unless physical segregation exists.
Name Email Phone Number Company Department State City 1 / 15 How does analytics support adherence to regulatory guidelines in the Indian pharmaceuticalmanufacturing sector? 2 / 15 In the Indian pharmaceutical industry, what does analytics-driven supply chain management primarily focus on?
Insights from USP’s Medicine Supply Map demonstrate that geographic concentration of pharmaceuticalmanufacturing anywhere in the world – including within the United States – increases the risk for drug shortages. Promoting geographic diversity of the manufacturing base of U.S.
billion in civil damages to states affected by the opioid crisis, which the Department of Justice said was the largest penalties ever levied against a pharmaceuticalmanufacturer. Purdue filed for bankruptcy last year, after it proposed a separate $10 to $12 billion settlement package to resolve those lawsuits.
However, despite this significant market share, the Japanese market is likely to become a less attractive market for international pharmaceutical companies based on recent findings from the Office of Pharmaceutical Industry Research (OPIR).
The information contained within the download document is intended for pharmaceuticalmanufacturers, 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.
For separate external shipping containers, USP has also reduced the need for plastic wrap and is evaluating smaller container sizes and biodegradable packaging materials, as well as a more easily recyclable alternative to EPS for cold-chain applications. In addition, they are more compact and 44% lighter than previous versions, on average.
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, pharmaceuticalmanufacturers are performing CCIT during commercial production to ensure that packaging processes are operating as they should.
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