Apollo AyurVAID, India’s leading NABH-accredited precision Ayurveda hospital network, announces its entry into the Ayurveda product segment, marking a significant step beyond clinical care. The new range includes classical formulations, OTC products, and medical foods, developed to meet the growing demand for safe, clinically validated Ayurveda …
Bayer has submitted a marketing authorization application to the European Medicines Agency (EMA) for gadoquatrane, its investigational MRI contrast agent. It is intended for contrast enhancement in MRI scans to detect and visualize suspected or known conditions across the body and central nervous system (CNS) in …
Lupin Limited (Lupin) and Zentiva Group (Zentiva), a pan-European pharmaceutical company, have entered into a license and supply agreement for commercialization of Lupin’s biosimilar Certolizumab Pegol, across multiple markets globally. This strategic alliance aims to accelerate the availability of high-quality, cost-effective biosimilar Certolizumab Pegol to patients …
Validation of compressed air used in pharmaceutical processes ensures the air meets quality standards, preventing contamination and ensuring product safety. Why Validate Compressed Air? 1. Prevents Contamination: Ensures air quality, preventing particulate, oil, and microbial contamination. 2. Ensures Product Quality: Maintains product integrity, stability, and efficacy. …
Pharmaceutical process validation involves verifying that a process consistently produces products meeting predetermined specifications and quality attributes. Here’s an overview of process validation with three consecutive production batches: Objective: Verify that the process is robust, consistent, and produces product that meets quality standards. Three-Consecutive-Batch Approach: 1. …
Here are some top formulation R&D interview questions for experienced professionals in oral solid dosage forms: Q1: How do you approach formulation development for a new API with poor solubility? A1: “I’d employ strategies like particle size reduction, solid dispersion, or complexation to enhance solubility. I’d …
Q1: What are flow properties of powders, and why are they important? A1: Flow properties refer to the ability of powders to flow smoothly and consistently. They’re crucial in industries like pharmaceuticals, food, and cosmetics, as they affect product quality, processing efficiency, and equipment design. Q2: …
Hi all , we are looking for below experienced candidates for QA department for our jadcherla location ,plz share resumes to bhaskara@sciegenpharm.com 1. Qualification/ Validation (5-8 years) Job profile: Experience Qualification – (PRD, Eng, WH, Mapping)/External calibration schedules Sending to instrument for external calibration from all departments …
Here are some potential interview questions and answers for MSAT (Manufacturing Science and Technology) or Tech Transfer department in Pharma: Q1: What is your experience with tech transfer in pharma? A1: “I’ve worked on several tech transfer projects, transferring processes from R&D to commercial scale. I’ve …
Here are some advanced questions and answers on Material Science and Technology (MS&T) in injectable plants: Q1: What are the key material considerations for injectable plant-based therapies? A1: Key considerations include biocompatibility, biodegradability, mechanical properties, and surface chemistry. Materials like PLGA, PLA, and PCL are commonly …
