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Gerresheimer, a systems and solutions provider for the pharmaceutical and biotech industry, has introduced a web-based product database designed to streamline the selection and registration of primary plastic packaging for medicinal products. It is constantly updated with new content and functionality to meet current and future needs.”
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
s CDC Vaccine Committee Overhaul for the Pharmaceutical Industry June 10, 2025 By Christopher Cole News Article The dismissal of all 17 members of the Advisory Committee on Immunization Practices has far-reaching impacts for the industry and beyond.
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.
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.
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).
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.
The new facility will feature state-of-the-art cleanroom packaging and high-sensitivity analytical testing capabilities. Communication between the manufacturing plant and retail stores. as part of the company’s commitment to providing a reliable supply of bioprocessing ingredients and excipients to the biopharma and pharmaceutical industries.
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,
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.
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
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.
Other PrEP regimens on the market require daily oral dosages or shots every few months, but the latest version is only administered twice a year. The FDA approved the updated formulation, which will be sold under the brand name Yeztugo, earlier this month.
With a portfolio exceeding 100 products, Sagent offers a wide range of options across various therapeutic categories, formulations, and packaging configurations, such as vials, syringes, and premix bags.
Recent Videos Related Content BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing. PharmTech.com , May 8, 2025.
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.
This article explores why E&L studies go wrong and how to build a submission-ready package from protocol to final report. How to get it right -A practical framework Start with a Risk Assessment: Map out materials, dosage form, route of administration, and expected interactions. Many Indian companies skip this step.
Tjoapack Announces Packaging, Cold Chain Expansions in US and Netherlands Patrick Lavery June 9th 2025 Article Most of the company’s new additions, if not already online, will be scheduled for commissioning, validation, or qualification before the fourth quarter of 2025.
Last month, European Commission approved the new subcutaneous (SC) formulation of Bristol Myers Squibb’s (BMS) Opdivo (nivolumab) with a dosage strength of 600 mg/vial, expanding treatment options for various adult solid tumours. Sign up for our daily news round-up! Give your business an edge with our leading industry insights.
Key parameters, such as pressure and orifice size, are carefully calibrated to achieve accurate drug delivery at the desired depth and dosage, making it a safe and efficient alternative to traditional needle injections. Additionally, clinical trials have been conducted to validate the safety and performance of N-FIS.
Recent Videos Related Content BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing. Press Release. June 12, 2025.
BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing. BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing.
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.
Spanning pharma machinery, packaging, analytical instruments, laboratory technologies, ingredients, and beyond, it offers a comprehensive platform for stakeholders to engage in transformative dialogues and foster strategic partnerships.
In the oral form, as a supplement, Glutathione should be consumed only in the recommended dosage prescribed by a doctor. Doctors have stated that the danger of getting these treatments from non-professionals could give rise to wrong dosage, faulty technique, or contamination.
A Novel, Enhanced, and Sustainable Approach to Audit Trail Review Diana Russo July 4th 2025 Article Eli Lilly and Company developed an innovative and sustainable approach to audit trail review (ATR) aimed at reducing the ATR burden while adhering to regulatory expectations and data integrity (DI) principles.
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Supported by the previous clinical demonstration of the safety profile of our innovative delivery technology and a solid pre-clinical package, we believe PST-611 holds the potential to improve both anatomical and functional features of dry AMD/GA.”
New Company Chrysalis Launches After Acquisition of Cleanroom Assets Patrick Lavery June 17th 2025 Article Chrysalis lists among its partners early-stage biotechnology companies, contract research organizations, top-10 pharmaceutical firms, and various other life sciences stakeholders.
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.)
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.
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.
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.
The proposed order is intended to significantly simplify the development of new dosage forms for oral monograph order drugs that, at this time, may be marketed only in tablets or capsules.
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.
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.
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.
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.
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.
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