Pyrogen Test

Pyrogen Test-How to Determine the Pyrogen Using Rabbits

Pyrogen Test- A pyrogen test is used to measure the presence of pyrogens in a sample. Pyrogens are substances that can cause fever, and the test is used to determine if a given substance is likely to cause this side effect. The test is performed by injecting a small amount of the substance into an animal, typically a rabbit, and then measuring the animal’s body … Continue reading Pyrogen Test-How to Determine the Pyrogen Using Rabbits

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Hold-Time Study for Pharmaceutical Products -Guidelines for Hold-Time Studies

Hold-Time Study for Pharmaceutical Products- A hold-time study aims to ensure that the medicinal product maintains its quality during storage and transport under the conditions specified on the label. The results of a hold-time study can be used to support the medicinal product’s stability and determine appropriate shelf life. There are several aspects to consider when designing a study to assess the stability of a … Continue reading Hold-Time Study for Pharmaceutical Products -Guidelines for Hold-Time Studies

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Event Tree Analysis? Event Tree Analysis in Pharmaceuticals?

Event Tree Analysis in Pharmaceuticals?- ETA is a top-down, quantitative risk analysis technique that uses a graphical representation of events and their associated probabilities to identify all possible outcomes of an event. ETA is commonly used in many industries, including the pharmaceutical industry, to evaluate the probability and impact of potential failure modes. What is Event Tree Analysis? This is a technique used to analyze … Continue reading Event Tree Analysis? Event Tree Analysis in Pharmaceuticals?

Purified Water System in Pharmaceuticals

Purified Water System in Pharmaceuticals? Why Purified Water is Required for Pharmaceuticals

Purified Water System in Pharmaceuticals? Pharmaceutical water systems are critical in manufacturing many drugs and medical devices. The water must meet certain purity specifications to ensure that it will not interact with the active ingredients or final product in a negative way. What is Purified Water? A purified Water System in Pharmaceuticals is essential to treat and remove impurities. Purified water is usually produced by … Continue reading Purified Water System in Pharmaceuticals? Why Purified Water is Required for Pharmaceuticals

Generic Drug Manufacturing

Generic Drug Manufacturing-India’s Position in Generic Drug Manufacturing

Generic Drug Manufacturing- The world’s generic drug market is estimated to be worth US$86.7 billion, and it is growing at around 8% per year. This rapid growth is being driven by the increasing demand for affordable medicines in developing countries and by the expiration of patents on many popular drugs in developed countries. India is one of the leading manufacturers of generic drugs, with a … Continue reading Generic Drug Manufacturing-India’s Position in Generic Drug Manufacturing

Good Manufacturing Practice training Course

Good Manufacturing Practice (GMP) Training Course

Good Manufacturing Practice (GMP) Training Course: Good Manufacturing Practice (GMP) is a critical step in ensuring the quality and safety of your products. The training course will teach you the basics of GMP and help you comply with regulations governing the manufacturing process. What is Good Manufacturing Practice? Good Manufacturing Practice (Pharmaceutical Compliance) is a set of standards that manufacturers should adhere to produce safe … Continue reading Good Manufacturing Practice (GMP) Training Course

Pharmaceutical Compliance Guide

Pharmaceutical Compliance Guide ? What is Good Manufacturing Practice?

Pharmaceutical Compliance: Pharmaceuticals are highly regulated and must meet certain quality and safety standards to be sold. This means that the manufacturing process of these drugs must follow specific guidelines known as Good Manufacturing Practice (GMP). In this Compliance Guide, we’ll outline what GMP is, explain why it’s essential, and provide a guide to its implementation in a pharmaceutical company. Pharmaceutical Compliance The pharmaceutical industry is … Continue reading Pharmaceutical Compliance Guide ? What is Good Manufacturing Practice?

What is Plate Exposure Method Exposure Methods?

What is Plate Exposure Method! Exposure Methods?

Petri plate exposure method is used in microbiology and plant pathology to cultivate microorganisms or plant cells. The method involves the deposition of an inoculum (a suspension of microorganisms or plant cells) on a surface covered with a solid medium, such as agar or cell culture medium. The medium will then spread the inoculum over the surface, allowing it to grow. After some time – … Continue reading What is Plate Exposure Method! Exposure Methods?

Disinfectant rotation

Disinfectant Rotation Validation Protocol? How does it Work?

Disinfectant rotation is changing the disinfectant used to regularly clean surfaces in an area. The rationale behind disinfectant rotation is that one disinfectant may not be able to kill all types of bacteria completely. Using different types of disinfectants, you can ensure that all surfaces in an area are appropriately cleaned and those dangerous microbes are removed. What is Disinfectant Validation? Disinfectant validation is the … Continue reading Disinfectant Rotation Validation Protocol? How does it Work?

Importance of Cleaning validation

What is the Importance of Cleaning validation?

Importance of Cleaning validation? Cleaning validation is a process used to ensure that cleaning procedures are effective in removing all traces of contaminants from equipment. This is important because contaminants can lead to product recalls, safety issues, and decreased efficacy of the equipment. What is cleaning validation? Cleaning validation is the process of verifying that a cleaning process (Disinfectant validation protocol) is effective in removing … Continue reading What is the Importance of Cleaning validation?