Category: Pharma Articals
Milestone Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has accepted for review the company’s response to the Complete Response Letter (CRL) for cardamyst (etripamil) nasal spray, an investigational therapy for paroxysmal supraventricular tachycardia (PSVT). The FDA has set a new Prescription Drug User …
Becton, Dickinson and Company, popularly known as BD, and Waters Corporation recently announced a strategic collaboration to combine BD’s Biosciences Diagnostic Solutions business with Waters’ expertise in analytical technologies. This joint venture aims to create a new life sciences and diagnostics entity focused on regulated, high-throughput …
Eli Lilly and Company (India), in collaboration with the Association of Physicians of India (API), has launched ‘API – Obesity Gurukul’, a Continuing Medical Education (CME) program aimed at helping physicians better manage obesity, which is becoming one of India’s major public health challenges. Taking inspiration …
There are several routes of drug administration, each with its own advantages and disadvantages. Common Routes: 1. Oral: Taken by mouth, absorbed through the gastrointestinal tract. 2. Parenteral: Injected into the body, either intravenously, intramuscularly, or subcutaneously. 3. Topical: Applied directly to the skin or mucous …
Role of the Technology Transfer Department in the Pharmaceutical Industry The Technology Transfer (TT) department is essential in moving pharmaceutical products from development to full-scale manufacturing. Their primary role is to ensure a seamless transfer of manufacturing processes, analytical methods, and technical knowledge from R&D to production, ensuring …
Lyophilization, also known as freeze-drying, is a process that removes water from a frozen product by sublimation, resulting in a dry, stable product. How Lyophilization Works: 1. Freezing: The product is frozen to a temperature that makes the water molecules form a solid crystal structure. 2. …
Merck today announced the initiation of the EXPrESSIVE Phase 3 clinical trials, evaluating the safety and efficacy of MK-8527, an investigational once-monthly, oral nucleoside reverse transcriptase translocation inhibitor (NRTTI) for HIV pre-exposure prophylaxis (PrEP). The EXPrESSIVE-11 trial will evaluate the safety and efficacy of MK-8527 among …
Forced Degradation Studies in Pharmaceuticals Forced degradation studies, also known as stress testing, are conducted to evaluate the stability of pharmaceutical products under various stress conditions. Purpose: 1. Identify Degradation Pathways: Determine potential degradation pathways and products. 2. Develop Stability-Indicating Methods: Develop analytical methods that can …
Sterilization methods in the pharmaceutical industry ensure products are free from microorganisms, ensuring safety and efficacy. Here are common methods: 1. Heat Sterilization: – Autoclaving (Steam Sterilization): Uses high-pressure steam to kill microorganisms. – Dry Heat Sterilization: Uses hot air to sterilize materials. 2. Filtration Sterilization: …
1. What are pharmaceutical pellets? Pellets are small, spherical, or semi-spherical solid dosage forms used in pharmaceutical formulations to ensure controlled drug release, improve bioavailability, and facilitate drug delivery. 2. What are the advantages of pelletization in drug formulation? Uniform drug distribution. Improved flow properties. Controlled …
Ad Blocker Detected
Our website is made possible by displaying online advertisements to our visitors. Please consider supporting us by disabling your ad blocker.
error: Content is protected !!
