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The worldwide pharmaceutical container packaging market is expected to rise in revenue from $104.12 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. billion in 2025 to approximately $174.45
WASHINGTON — Amid a scramble to assemble a health care policy package in the Senate, a pair of key senators have significantly changed a proposal to cap insulin costs. The new legislation by Senate Diabetes Caucus co-chairs Sens. Jeanne Shaheen (D-N.H.)
ACG Packaging Materials has received the First Export Award in the category of Plates/Sheets/Films/ Etc. ACG Packaging Materials aims to maintain the quality and integrity of pharmaceutical and nutraceutical products, by protecting them from environmental factors such as moisture and oxygen.
A batch of Labetalol 200mg tablets has been recalled as they are incorrectly labelled as 100mg tablets on the foil blister packaging. Pharmacists have been instructed to immediately stop […] The post Labetalol batch recalled due to wrong dosage labelling appeared first on The Pharmacist.
For most consumers, product packaging represents their first impression of a brand and its sustainability credentials. But how is this push shaping the pharma packaging market and what are the key changes we can expect to see? For many, aesthetic appeal and user experience top the list of priorities when it comes to packaging design.
If a package coalesces, it likely would not be introduced until next year. PTO’s Patent Trial and Appeal Board said that Mylan had shown a reasonable likelihood that the Novo patent covering dosage regimes for the drugs was invalid. The committee has jurisdiction over Medicare and Medicaid payment policies for hospitals.
In a recent paper, published in the International Journal of Pharmaceutics , researchers identified nitrocellulose blister packaging as a potential source of N -nitrosodimethylamine (NDMA) and N -nitrosodiethylamine (NDEA) impurities.
ACG’s unique value lies in our holistic approach to the pharma industry, a journey that started 60 years ago with capsules and has since expanded to include everything from filling machines and packaging to advanced supply chain technology like the Life Sciences Cloud. The answer is all of the above.
If you have ever taken any kind of medication, be it prescription or over the counter (and you almost certainly have), then you’re probably familiar with blister packaging. Blister packaging is extremely common in the pharmaceutical industry, thanks to its many benefits. Intuitive Dosage. Convenience. Regulate Routine.
These launches form part of Morepens broader strategy to enhance its finished dosages segment while leveraging its internal research and development (R&D) capabilities. The product is offered in a 4×14 patient-compliant pack with day/night markers and matte foil packaging. The company notes its 98.23
NOTE: The dispensing label must not obscure the active ingredient(s), strength, and expiry date as printed on the manufacturer's packaging. drug dosage) and the indications of medication (e.g. Complete the course" for antibiotics, "May cause drowsiness" for sedating drugs, etc.) fever, cough or cold).
As environmental concerns continue to intensify, the pressure on the pharmaceutical industry to reduce its overall environmental impact, particularly in final dosage forms, is growing proportionately.
Step 2: ANDA Filing Generic drug manufacturers submit an Abbreviated New Drug Application (ANDA) to the FDA, which includes detailed information about the proposed generic drug, including its active ingredients, dosage forms, and manufacturing processes. This includes providing clear instructions for use, warnings, and precautions.
The event will gather the entire supply chain, including ingredients, finished dosages, machinery, bio, and packaging. CPHI Europe, reportedly, the world’s largest pharmaceutical event, will return to Messe Frankfurt from October 28-30, 2025. CPHI events highlight industry trends, with analysts predicting growth in 2025.
Subscribe on iTunes , Android , or Stitcher If you navigate to the page on the website for the Institute for Safe Medication Practices that once hosted the document titled “Oral Dosage Forms That Should Not Be Crushed” you will instead find a notice that the list has been removed from the ISMP website.
This enables us to optimise dosages in our final products, enhancing both bioavailability and patient safety. Some of our clients have successfully implemented strategies such as displaying supplier logos and QR codes on packaging, allowing consumers to easily access information about the ingredients and clinical results.
Pharmaceutical companies are looking to paediatric indications of approved adult dosage forms (ADFs) to sustain and fuel growth. Various modifications to adult dosage forms (ADFs) are often needed to make a drug easier for children to take and easier for parents to administer. Innovative solutions to complex challenges.
Manufacturers are actively looking at ways they can improve drug delivery through well-designed parenteral packaging systems, and the choice to deploy prefilled syringes for more and more injectable drug products is a key part of this push. Prefilled syringes offer a number of advantages over the more traditional glass vial.
Lupin Limited – Openings for PDL (Process Development Lab) & Packaging Development Department -Apply Now. We have Urgent Requirement for PDL (Process Development Lab) & Packaging Development Department for our Pithampur Location. Department: PDL (Process Development Lab) & Packaging Development. Job Description.
Stability tests are designed to assess the percentage of the active substance throughout the products shelf life and provide insight into any degradation that may occur within the final dosage form. For solid dosage forms, including capsules, tablets, or film-coated tablets, dissolution tests are conducted.
Pharmaceutical Technology Europe spoke with Ali Rajabi-Siahboomi, vice president and chief innovation officer at Colorcon, about the evolution of coating design and how it has impacted investment, as well as innovations in packaging for oral solid dosage products.
IPA also pointed out that US regulations require adverse events related to any dosage form of a drug to be reported under the same Abbreviated New Drug Application (ANDA) number, even if the product is manufactured at a different facility or outside India. Thus, it cannot be conclusively linked with the manufacturing site or manufacturers.
The ADAPTA 50 capsule filler features innovative technical solutions to manage complex solid dosage forms such as product combination in hard gelatine capsules or powder micro-dosing for Dry Powder Inhalers. End-of-line solutions, from robotics, handling, overwrapping to case-packing and palletising are provided by the IMA EOL hub.
CPHI, the global pharmaceutical event that spans the entire supply chain from ingredients and finished dosages to machinery, bio, and packaging will return to Fiera Milano (Rho) in 2024.
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.
Sachets are a popular pharmaceutical and nutraceutical packaging format for consumers and manufacturers alike. To ensure accurate dosage and administration, the powders used in these delivery systems require excellent flowability.
Bhatkar covered the requirements for sterile dosage manufacturing and the coordination between actuation and architectural design. Topics included the management of HVAC systems during shutdowns, power failures, and secondary packaging unit requirements. He also referenced the WHO guidelines included in the Revised Schedule M.
OTC drugs come in various forms, including tablets, capsules, creams, and liquids, and are generally labeled with clear instructions on proper usage and dosage. Its OTC drug section covers a broad range of OTC medications, offering detailed descriptions, recommended dosages, and potential drug interactions.
Documentation : Keeping detailed records of orders, specifications, manufacturing processes, packaging, and labeling to ensure traceability and compliance. Packaging and labeling operations for investigational products are often complex and must meet specific requirements to ensure the integrity of clinical trials.
Counterfeit drugs, intentionally mislabeled or misrepresented, often contain substandard or harmful ingredients, incorrect dosages, or no active ingredients at all. The introduction of track and trace systems, facilitated by unique identification codes on drug packaging, has played a vital role in multiple ways.
The impact of packaging is felt only when it does not do its job and therefore pharmaceutical companies have traditionally invested quite a bit on product packs, also using them as part of their branding strategy. sq mm of material – there is more than 20 per cent reduction of packaging material. per cent CAGR. Shivshankar S.R,
Societal™ CDMO is a bi-coastal contract development and manufacturing organization (CDMO) with capabilities spanning pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms with a primary focus in the area of small molecules
The Popit Sense device can be clipped to just about any kind of medicine blister sheet, which is the most common form of packaging for oral solid dosage (OSD) drugs globally. “While typically patient data is only collected up to the point of prescription, we can now support patients throughout their treatment in real-time,” he added.
Subscribe on iTunes , Android , or Stitcher If you navigate to the page on the website for the Institute for Safe Medication Practices that once hosted the document titled “Oral Dosage Forms That Should Not Be Crushed” you will instead find a notice that the list has been removed from the ISMP website.
Amber Specialty Pharmacy employs pharmacists who have specialized training in transplant care and review each patient’s medications to prevent any drug interactions, as well as adjust medication dosages to help with side effects. Amber Specialty Pharmacy, a Hy-Vee, Inc.
They’re designed to be bioequivalent, meaning they have the same dosage, strength, route of administration, quality, and intended use as the original brand-name drug. Generic drugs are pharmaceutical products that contain the same active ingredients as their brand-name counterparts.
The events cover every step of the pharma supply chain: ingredients, machinery, equipment, technology, package and contract service suppliers, distributors, and buyers from the pharmaceutical industry.
The regulatory package submitted to the EC included evidence derived extensive analytical characterisation. Tyruko ® has the same strength/dosage form, intravenous (IV) route of administration, dosing regimen and presentation as the reference medicine, according to Sandoz. Tysabri ® is a registered trademark of Biogen MA, Inc.
The combination reduced the dosage of the two drugs and “demonstrated improved antimicrobial and anti-biofilm properties”. Specifically, the two small molecule drugs were studied against the pathogens Staphylococcus aureus , Escherichia coli , and Candida albicans. allicin and domiphen] reduced the total viable counts of E. coli and C.
To achieve this, startups should implement rigorous quality control measures throughout their production processes, from sourcing ingredients to manufacturing and packaging. This includes accurately labelling their products with all required information, such as ingredients, dosage recommendations, and potential allergens.
Issues with regulatory requirements and documentation can also cause significant delays, while any inaccuracies in translations on labelling can mean that dosage and storage information is not correctly understood or followed. Upcoming biotechs need to get moving and they don’t have time to wait for a packaging slot for eight months.
Pharmaceutical solid dosage forms are the most popular in the pharmaceutical industry and are one of the most used drug delivery methods across patient groups. Growth of oral solid dosage contract manufacturing in the pharmaceutical industry. Find the leading pharmaceutical solid dose manufacturing companies in contract marketing.
Understanding both the significant competitive advantages that FDC products can offer, and the difficulties and potential pitfalls associated with development and manufacturing of FDC drugs in oral solid dosage forms is a critical first step for companies exploring this approach. Of those 131 approved FDCs, 98 were oral dosage forms.
Pharmaceutical compounding is a method of preparing personalised medications for patients by mixing the individual ingredients in the exact strength and dosage form required by the patient. Packaging. • It may provide access to discontinued drugs and allows for alternative compounded dosage forms. Excipients. Formulation.
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