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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.
PHARMAP 2023 gathered pharma companies, CMOs and CDMOs, governmental bodies to exchange experience in digital transformation and discuss innovative solutions and business practices. The next edition of the PharmaceuticalManufacturing and Packaging Congress 2024 is going to take place on 22-23, April, in Amsterdam, the Netherlands.
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. lakh crores) in the 2022–2023 fiscal year. lakh crores) in the 2022–2023 fiscal year. billion (Rs 2.1
Leaders of the whole pharma value chain meet at PharmaceuticalManufacturing and Packaging Congress (PHARMAP) to find new connections and discuss trends of the industry. Mohamed Chalal, New Product Introduction Manufacturing Sr.
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.
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.
Revised for 2023, the Parenteral Drug Association (PDA) has published an update to its Technical Report No. 43: Identification and Classification of Nonconformities in Moulded and Tubular Glass Containers for PharmaceuticalManufacturing.
This way the business program of PHARMAP 2023 is created to discuss and examine new trends for reshaping the pharma industry. COVID-19 has sped up the digital transformation and forced pharmaceutical companies to rethink many aspects of their business. Sustainability topic, you see that a lot of changes are going on with the packages.
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.
While it officially applies to the manufacture of sterile medicinal products in the European Union, the revised EU Good Manufacturing Practice (GMP) Annex 1 effectively reset the benchmark for quality standards across the globe on 25 August 2023. Register your details to read more The post How ready are you?
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.
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.
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.
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.
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).
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., josh.levin@usp.org Thu, 08/03/2023 - 15:43 Supply Chain
Importantly, these efforts can provide USP Convention Member organizations and Expert Volunteers with even more transparency on the impact we are collectively making to improve global public health, bolster environmental sustainability of the pharmaceutical supply chain, and build trust in science-based institutions like USP.
Some of their thoughts are: Mr. Mekala Rao (Chairman – Technology Global PHT Expo & Summit – 2023 and President – Atachi Systems, USA) – “motivation to attend Global PHT is to understand the cultural gap in the production of innovative medicine, healthcare systems between eastern and western world.
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).
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.
Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: June 3, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.
Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: May 28, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.
In the five years between 2019 and 2023, the FDA issued the following warning letters, closely related to ineffective deviation investigation. Adulterated Pharmaceuticals: 396 warnings iii. Packaging/labeling/Misbranding: 41 warnings vi. CGMP Deviation: 39 warnings ii. Adulterated API: 39 warnings iv.
Packaging material specifications In the pharmaceutical industry, the requirements for pre-printed packaging materials must be well-defined and documented to ensure that you get the items you specified or ordered and that there are no mix-ups. A standard name and a unique item code define packaging materials.
Particularly the printed packaging materials where product information is presented. Printed packaging materials typically include product names, active ingredients, concentration, batch numbers, expiry dates, registration numbers, barcodes, etc. Commonly used packaging materials are cartons, inserts, leaflets, printed foil, etc.
This indicates that, despite some progress, a significant portion of the sector still needs to elevate its ESG practices, as per an October 2023 report from Deloitte, titled, ‘Embedding environmental sustainability into pharma’s DNA’. Embedding sustainability into the core business strategy is essential for long-term success.
The 16 th edition of CPHI & PMEC India Expo, organised by Informa Markets in India, will be held from November 28-30, 2023, at the India Expo Centre in Greater Noida, Delhi. The post 16th edition of CPHI & PMEC India Expo to be held from November 28-30, 2023, at India Expo Centre, Greater Noida appeared first on Express Pharma.
Amidst numerous warning letters distributed by the US Food and Drug Administration (FDA) to pharmaceuticalmanufacturers in recent months, in July this year, the US regulatory body published its analysis on drug product quality in 2022. Edge Biologicals Inc., An FDA warning letter delivered to Edge Biologicals Inc.
To keep the EU’s medicine supply intact, Gupta suggests governments should adopt new pricing policies and provide further aid to mitigate the impact of rising operational costs; they should also minimise the exodus of generics manufacturers.
In this article, we will discuss important aspects of equipment cleaning that are required during pharmaceuticalmanufacturing. In other areas, such as in secondary packaging or in material storage areas, the product isn’t exposed to the environment, so there is a lower risk of contamination.
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