What Are Blood Glucose Regulators? Understanding the Science Behind Blood Sugar Control

In this blog we will learn about blood glucose regulators, also known as blood sugar regulators. In general, they are the chemical substances or hormones that are responsible for the maintenance of sugar levels in the blood. 

Safe regulation of glucose/sugar in the blood is one of the most important biological processes in the human body. Every second, our body carefully balances blood sugar levels to provide energy to cells; at the same time, it protects the organs from damage caused by excessive glucose.

In the situation where this balance is disrupted, it can lead to serious health conditions such as diabetes, obesity, metabolic syndrome, cardiovascular disease, and nerve damage.

Thus, in these scenarios, blood glucose regulators become critically important.

How Do Small Research Chemical Companies Support Global Healthcare Innovation ?

In the pharmaceutical industry, a number of organizations work collaboratively in the search and development of safe medicines.

Large organizations work on the big picture to solve the problems; however, the smaller organizations work on technical precision and flexibility. 

The small organizations play a crucial role in the pharmaceutical developments. They provide technical support in chemical synthesis and analytical method developments.

Specifically the small organisations are helpful for

• Custom synthesis
• API intermediates
• Pharmaceutical Impurities
• Reference Standards
• Nitrosamine Impurities

Thus, the small organizations provide their indirect contributions to global healthcare innovations.

The following presentation provides an overview of the contribution of the small research chemical companies in delivering healthcare solutions.

This presentation will serve as a valuable guide for graduate students aspiring to build successful careers within the pharmaceutical industry.

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Please read the original article here: https://medium.com/@srborkar/how-small-research-chemical-companies-support-global-healthcare-innovation-f6c7063cf97c

Forced Degradation Studies Explained: Identifying Drug Impurities Step-by-Step

What are forced degradation studies?

Here in the following video a step-by-step explanation is given. This provides a brief overview of forced degradation studies, their impact, and their importance in the regulatory submissions of the drug products. This is helpful for the graduate students and industry professionals who want to pursue a career in the field of pharmaceuticals. 

This video answers following questions:

What are API impurities?

What are the forced degradation studies?

What is the need for forced degradation studies for the new drug product?

What are the analytical tools required for these studies?

What is the impact of forced degradation studies?

Check out our other articles for more details about API impurities. 

1) Forced Degradation Studies for Drug Impurity Identification Explained

2) Control Strategy for API Impurities: Best Practices for DMF Filing

3) Identification, Characterization, Synthesis, and Isolation of API Impurities: A Comprehensive Guide

 

The synthesis of pharmaceutical impurities and reference standards is essential in the drug manufacturing process and regulatory submissions of the new drug formulations. The API impurities are specifically required for the analytical method developments, understanding the impurity profile of the API. Also, the mutagenic impurities, like nitrosamine impurities, need to be identified and characterized during the regulatory submissions of newly developed drugs. 

Watch the video on YouTube: https://www.youtube.com/watch?v=u35fV2P_S1s