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The Indian Pharmaceutical Alliance (IPA) questions the reliance on the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) in the Ohio State University report titled, Are All Generic Drugs Created Equal? An Empirical Analysis of Generic Drug Manufacturing Location and Serious Drug Adverse Events.
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.
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. In March 2024, Lonza hosted its first digital Responsible Supplier Event which brought together more than 1,100 participants.
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. This year’s event marks the 20th anniversary of the CPHI Pharma Awards.
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. customers will have the opportunity to experience first hand various digital solutions aimed at reducing maintenance costs and downtime.
The event attracted over 200 attendees and continued the PULSE series’ role in providing a platform for industry learning. Bhatkar covered the requirements for sterile dosage manufacturing and the coordination between actuation and architectural design. The session began with a keynote address by Thiru M.
CPHI is a global platform that unites over 100,000 professionals from the pharmaceutical industry, hosting events in Spain, North America, the Middle East, India, Southeast Asia, Japan, and Korea. The team’s main goal at the event was to meet local medical companies in advance and explore their needs.
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.
Introduction Medication error is any preventable event that may harm patient. Also, similar packaging design across medication strengths can lead to inadvertent selection errors, potentially impacting patient safety. This highlights the importance of double-checking unfamiliar dosages to prevent potentially serious medication errors.
Biopharmaceutics is a scientific discipline that examines the interrelationship of the physicochemical properties of the drug, the dosage form in which the drug is given, and the route of administration on the rate and extent of systemic drug absorption ( Applied Biopharmaceutics and Pharmacokinetics, Shargel, Wu-Pong and Yu, 5th Edition ).
Starting materials are processed, sampled, tested, packaged, and released before the finished products are stacked on pharmacy shelves. Sampling is carried out on intermediate processed materials and tested to ensure those are formulated correctly, free from contamination and qualified for filling and packaging. as their visual aids.
Out of trend results What is the origin of out of specification events? The court ruled that any individual OOS event should be investigated, and if a laboratory error cannot be identified, the batch will fail the test. Subscribe What are the typical sources of out of specification events?
The analyst should ensure that the supervisor is notified as soon as an OOS event occurs, the sample is retained, and a documented investigation is commenced. Dealing with out-of-specification results Laboratory result out-of-specification events are a common occurrence in the quality control process.
These events led to the publication of the EU Pharmaceuticals Strategy in 2020, 1 which, in addition to a range of other activities, aims to ensure the regulatory system for human medicines is future? It is too early to say because we have not seen the whole package of measures yet. Future outlook.
With the Indian pharma market projected to grow to $ 130 billion by 2030 and $ 450 billion by 2047, the event highlighted the industry’s vital role in shaping global healthcare. Unveiling excellence in pharma Day 1 of the event showcased the Pharma Connect Congress, which addressed pivotal themes shaping the pharmaceutical landscape.
Out of the 550+ reported counterfeiting incidents, either customs seizures or police/health inspector raids were involved, and 60% of the seizures comprised more than 1,000 dosage units. This amounts to more than 300,000 doses of counterfeit drugs intercepted. kristine.gates… Wed, 06/14/2023 - 08:16 Supply Chain
Follow package instructions. Follow package directions for each supplement. This can be used in the event of food poisoning, accidental ingestion of a food you’re sensitive to, or for binding mycotoxins and other pathogenic gut infections. The herb itself can be poisonous if ingested. and magnesium citrate before bedtime.
– Disintegration Testers (Critical for assessing the disintegration properties of solid dosage forms). – High-Speed Tablet/Capsule Counting Machines (Critical for accurate counting and packaging of tablets and capsules). . – Sterilization Autoclaves (Critical for ensuring aseptic conditions and product safety).
When the raw materials, components, and packaging materials arrive from the supplier, the first thing you should do is verify the goods match with records such as purchase order and delivery docket. It is important to assign in-house lot numbers for every container received next to the supplier’s lots of raw materials or packaging materials.
It also bears extra replacement expenses when drugs are discarded due to improper packaging. Hidden expenses can pile up, spiraling out of control due to many reasons related to supplier performance: the lack of appropriate documentation, storage, wrong dosage forms, and the list goes on.
I once took a nap in undergrad at a crowded bar, during a daytime event (and this was without any alcohol!). Put all of your worries, fears, and events of the day on paper, without judgment. Be sure to follow the package directions and your practitioner’s guidance to determine the right dosage for you.
This is key to achieving desired healthcare outcomes [2] Bane areas such as inaccessibility, labelling errors, dosage errors, and counterfeit drugs, must be addressed to make pharma packaging more patient-centric [3] One solution fits all is not the right approach.
While it’s uncommon for people without celiac disease to completely stop taking thyroid medication solely by going gluten free, some do find they can reduce their dosage through a gluten-free diet. You can learn about the top probiotics that I recommend at the linked to article, along with dosage info and precautions.
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