Pharmaceutical formulations are the specific compositions and preparations of API (s) and excipients. These formulations are designed to ensure the safe and effective delivery of medications. There are several types of pharmaceutical formulations, each tailored to meet specific patient needs and drug characteristics. Here are some common types of pharmaceutical formulations: Tablets and Capsules:…
Gummy vitamins have become increasingly popular as an alternative to traditional pill or capsule supplements,. They are typically made from gelatin, corn starch, sugar, and lots of fillers and chemical additives. But like any product, they come with their own set of pros and cons. It’s essential to consider these factors before deciding whether gummy…
Human performance errors in analytical laboratories are more common than we think! Let’s dive into some of the most common errors that can impact the accuracy and reliability of analytical results. Data entry errors: Accurate data entry is crucial for reliable analysis. Incorrectly entered data can lead to misleading results or flawed analysis. …
Process Capability & Performance Indicators (Pp, Ppk, Cp, Cpk) are specification indicators relative to process dispersion and process centering. Process capability is a statistical measurement of a process’s ability to produce parts within specified limits consistently, to meet the design specification for a service or a product. Process capability is expressed as 6σ,…
WHAT IS VALIDATION? EU GMP – it is “Action of proving, in accordance with the principles of Good Manufacturing Practice (GMP), that any procedure, process, equipment, material, activity or system actually leads to expected results. WHAT IS QUALIFICATION Performed to establish evidence that process equipment and ancillary systems are capable of operating within established…
QbD, or Quality by Design, is a systematic approach to pharmaceutical development and manufacturing that aims to ensure product quality by design, rather than by testing and inspection after production. But the principle of QbD can be applied to all stages of the product lifecycle, from research and development to commercial production. Key Components…
Process validation is a critical and mandatory step in the pharmaceutical industry to ensure the consistent production of high-quality pharmaceutical products. It is a systematic approach used to confirm that a manufacturing process consistently produces a product that meets its predetermined specifications and quality attributes. Process validation helps in ensuring patient safety and product…
Pharmaceutical Packaging encompasses the process of designing and developing primary, secondary, and tertiary packaging for pharmaceutical products, ensuring their safety, integrity, and quality. It plays a crucial role in protecting medications from factors like moisture, light, air, and contamination. With advancements in technology, pharmaceutical packaging has evolved to incorporate features like child-resistant caps, tamper-evident…
