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The 3rd edition of Pharma Live Expo & Summit will be held from April 17 to 19, 2025, at the Bombay Exhibition Centre, Mumbai. Pharma Live Expo & Summit 2025 provides a unique platform for stakeholders across the pharmaceutical value chain to come together, exchange knowledge, and drive impactful advancements.
Looking ahead to 2025, were witnessing an industry in transformation. 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.
LOG Pharma Primary Packaging is set to present its new barrier eco line at Pharmapack Europe 2025. LOGs barrier packaging solutions are designed to prolong shelf life and protect innovative and generic drugs from the exposure to moisture and/or oxygen, the company explained on its website.
The worldwide pharmaceutical container packaging market is expected to rise in revenue from $104.12 billion in 2025 to approximately $174.45 billion by 2033, according to a study published by Towards Packaging. Specifically, the “high quality of biodegradable and recyclable packaging materials” are driving the market.
By Sara M Keup In reviewing some new 2025 pharmacy rules/laws a couple interesting changes caught this bloggers attention: As of December 30, 2024, Missouri has rolled out new rules related to prescription drug delivery requirements. Massachusetts will begin enforcement against non-licensed pharmacy dispensing beginning on May 1, 2025.
PHARMAP 2025, Europe’s premier pharmaceutical congress, brought together over 300 senior leaders from major global pharma companies, including Bayer, Roche, Johnson & Johnson, AstraZeneca, Novartis, Novo Nordisk, Pfizer, Takeda, and more. The future of pharma is not just being discussedit is being actively shaped.
Pharmaceutical Technology sat down with Stefan Verheyden, Global Vice President Sales Pharma & Biopharma Solutions Injectables at Gerresheimer, to talk about the primary and secondary packaging solutions Gerresheimer and Bormioli Pharma will be showcasing at Pharmapack Europe 2025 in Paris, France from January 2223.
The agreement stipulates that certain conditions must be met in the labelling and packaging of these medicinal products. The following new measures are set to be introduced on 1 January 2025. After this date: Under the framework, medicines can have the same packaging and labelling across the UK.
CPHI Europe, reportedly, the world’s largest pharmaceutical event, will return to Messe Frankfurt from October 28-30, 2025. The event will gather the entire supply chain, including ingredients, finished dosages, machinery, bio, and packaging. CPHI events highlight industry trends, with analysts predicting growth in 2025.
Award winners by category DELIVERY AND DEVICE INNOVATION SHL Medical for Elexy reusable electromechanical autoinjector ECO-DESIGN WINNER Huhtamaki for Omnilock Ultra PAPER PACKAGING INNOVATION WINNER Mitsubishi Gas Chemical Company for new OXYCAPT Multilayer Plastic Vial PATIENT-CENTRIC DESIGN WINNER UCB Pharma for Bimzelx 160mg 2ml autoinjectors product (..)
Pharmaceutical Technology spoke with Peter Belden, president of Tjoapack US, ahead of DCAT Week 2025 to discuss recent innovations in bio/pharmaceutical packaging.
As we approach 2025, emerging trends are reshaping how the industry engages with patients and healthcare providers. From eco-friendly packaging to socially responsible campaigns, sustainability resonates with today’s consumers. Learn more about compliance tips at Pharma Marketing.
he Authentication Solution Providers Association (ASPA) conducted its MEA Open House on April 24 2025 at Anantara Downtown Dubai. The event brought together 46 delegates representing 17 companies from the authentication, packaging, and brand protection industries. The session began with an address from Manoj Kochar, President of ASPA.
Your Roadmap to Category Management Success in 2025 priyanka.katke… Mon, 11/18/2024 - 17:57 Your Roadmap to Category Management Success in 20252025 will feel familiar, in some regards. To prepare for all eventualities, grab your copy of the GEP Spend Category Outlook Report 2025.
Morepen Laboratories has announced the launch of four new productsTicapen, UdoFix, LycoMore, and Acifix Raftin April 2025 for the Indian market. The product is offered in a 4×14 patient-compliant pack with day/night markers and matte foil packaging. It is packaged in glass bottles and includes a dosing cap.
The notification, dated 15 April 2025, was issued under Section 26A of the Drugs and Cosmetics Act, 1940 (23 of 1940), citing the potential risk of using the said FDC in children under four and the availability of safer alternatives. Subsequently, the Drugs Technical Advisory Board (DTAB) also reviewed the safety of the combination.
Jayakumar gave examples of common issues, such as packaging damage or consistency problems in ointments, stressing the importance of not dismissing seemingly minor complaints, as they could escalate into more significant quality issues.
For example, on April 19, 2025, CDSCO published three lists of Not of Standard Quality (NSQ) drug alerts for March 2025, spanning 131 product batches. There is growing concern that a sizable proportion of medicines in India could be unsafe for patients. The most common reason cited is failing the dissolution test as per IP 2022.
According to the pharma company , the financing will add to global capacity: from manufacturing of active pharmaceutical ingredients (API) through to packaging. The construction projects will be finalised from the end of 2025 through to 2029. Most of the investment will be focused on API capacity.
The introduction of Velocity Vials will contribute to the ongoing evolution of our offerings and services and will expand our portfolio of high-quality tubular glass packaging. Pharma tubing production is expected to begin in 2025. Manufacturing of Velocity Vials at SGD Pharma’s facility in Vemula, India, is expected to begin in 2024.
.” Harshit Shah, President of IPMMA, remarked, “Pharma Pro&Pack Expo 2024 has once again demonstrated its critical role in driving innovation and collaboration across the pharmaceutical processing and packaging sectors. ” Exhibitors and visitors shared positive feedback about the event’s success. .”
June 6, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook The funds will support clinical milestones along with AI-driven development across Juvenescence’s portfolio. The acquisition forms a key part of Juvenescence’s partnership with the Abu Dhabi global healthcare company M42, which was announced in April 2025.
The second facility for WuXi STA in the US, Phase I of the new campus will provide formulation development, clinical and commercial drug product manufacturing services for a variety of oral and injectable dosage forms, as well as packaging, labelling, storage and distribution services for clinical trial materials and commercial drug products.
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. Read this case study to learn how a global pharmaceutical leader fixed inefficiencies in a 25M packaging budget.
CPI confirmed that the centre will establish operations during 2024 and be finished in late 2025. This is a first-of-its-kind collaboration for the pharma industry. Partners include AstraZeneca, GSK, and the University of Strathclyde. The project will be jointly funded by the UK and Scottish Governments.
June 6, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook The authorisation in the EU signifies a step forward in eye care for paediatric patients. Credit: chaponta/Shutterstock. Give your business an edge with our leading industry insights. Login Registration is disabled.
Over the years, we have continued to seek improvements to existing molecules to better meet patient needs – we have introduced novel heat-stable generic formulations, more convenient packaging options, and paediatric therapies.
June 9, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook The partnership will expand treatment options for mental health in the US. Preparations are underway to introduce Exxua into the US market swiftly, aiming for pharmacy and patient access by late 2025. Credit: Coco Ratta/Shutterstock.
and Europe held manufacturers accountable for their environmental impact, leading to an increase in partnerships with tech companies focused on sustainable packaging and production solutions. What are the top 3 trends to watch out for in 2025,which could have a disproportionate impact on the globaland Indian life sciences landscape?
The American Conference Institutes 12th Annual Legal, Regulatory, and Compliance Forum on Cosmetics & Personal Care is scheduled to take place from March 27-28, 2025, at the New York City Bar Association, New York, NY.
Alex Watt June 9, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook The delays in market access in individual EU member states have been an obstacle to the industry. Credit: New Africa via Shutterstock. times more products than the overall European average. Give your business an edge with our leading industry insights.
package insert. by the 2024/2025 respiratory virus season,” the statement informs. A follow-up analysis of the primary endpoint was performed during FDA review, including cases that started before the primary analysis cut-off date but were not confirmed until afterward. The results were consistent with the primary analysis [VE 78.7
For regulatory approval in Europe, Cellectar has submitted a comprehensive data package to EMA that includes preclinical findings, regulatory details, manufacturing information, as well as safety and efficacy data from the CLOVER WaM Phase IIb clinical trial.
The plant is specialised in the purification and filling of plasma-derived therapies, with packaging capabilities for a variety of plasma treatments. People with these conditions may require lifesaving treatment for acute emergencies, as well as lifelong substitution therapy.
Given that multiple work packages may often start or end together, or else take longer than others ( Figure 1 ), the introduction of new PAT requires assessment and planning by multiple departments. Figure 1 : Process analytical technology implementation in (bio)pharmaceutical GMP manufacturing. Bhatnagar A, Yadav S, Achanta V, et al.
June 9, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook YOLT-101 will be a new treatment possibility for familial hypercholesterolemia. Credit: aipicte/Shutterstock. Give your business an edge with our leading industry insights. Thank you for subscribing View all newsletters from across the GlobalData Media network.
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