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Pricing Strategy Consulting Firms

Additionally, the advantages of a more strategic approach to pricing could be seen right away. In spite of this, most companies lose money because they don’t set the right pricing or make sure that customers pay it. There are various reasons

Healthcare and Life Science Validation

Validation is the most used and common term to verify the GxP systems, whether they are in systems or in labs. All the required precautions should be followed and maintained every time to keep the system compliant that is used directly

What Has Changed Over the Years in Regulatory Affairs

The regulatory affairs role in the pharmaceutical industry is rapidly changing, with many of the tasks once aligned with in-house experts being outsourced or automated by developing technology. This trend is forcing industry professionals to rethink their role and establish themselves

Career In Regulatory Affairs

What is Regulatory Affairs? Regulatory affair is a profession within regulated industries such as pharmaceuticals, biopharmaceuticals, medical devices, cosmetics and consumer health, natural health, and veterinary products. A regulatory affair is a department within the company that interacts with the government

Quality Control and Assurance

The words quality assurance (QA) and quality control (QC) are sometimes used interchangeably. Although the two notions are similar, there are significant variances between them. This article will define and provide instances of the differences between quality control and quality management.

6 Essential Skills of a Regulatory Affairs Professional

The demand for regulatory affairs (RA) professionals is clearly evident across the pharma industry, consultancy companies, clinical research organizations, and regulatory agencies. As I was deciding on my career transition from being a laboratory scientist to a regulatory affairs specialist, I

Five Advantages of QA for Better Manufacturing

Five advantages of QA inspections: Numerous advantages of quality assurance are available to the organisation as well as the clients. The QA should be implemented for the following reasons: 1. Increasing the effectiveness of production When all manufacturing components are in

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