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The Power of a Document Management System in the Pharmaceutical Industry
“If it’s not written down, then it didn’t happen”. Considering the context of our blog topic, this proverb fits perfectly. In the pharmaceutical manufacturing, documentation
What are the Different Methods of Document Version Control?
In the fast-paced world of business today, document management is vital for productivity and compliance. Document version control, also known as versioning, plays a pivotal
Types of Audits in Quality Management
Quality audits assesses how well a product, design, process, or system meets specified standards or procedures. The auditors can perform quality audits both within the
Simple Guide to SOP Management in Pharma Industry
The complexity of manufacturing, especially in the pharmaceutical industry, is multifaceted and significantly high. The direct impact of pharmaceutical products on consumer wellness and health
What is CAPA in the Pharmaceutical Industry?
CAPA is Corrective and Preventive Action, holds immense significance in the pharmaceutical industry. The purpose of CAPA is to identify, analyze, and address problems by
Best Practices of Quality Management for Electronic Industry
The rapid growth of the electronic market encompasses a vast array of products and components for diverse applications, including consumer electronics, aerospace, automotive, and medical
Difference between QMS and ERP: Key Aspects and Functionalities
Comparing QMS Software (Quality Management System) and ERP Software (Enterprise Resource Planning) is akin to contrasting apples and oranges. Both fall into the broader category
What is Non-Conformance Software?
What if a food processing plant finds that the packaging of one of its products was contaminated with bacteria during production? Or, the pharma company
Essential Elements of Food Quality Management System
The globalization has made the manufacturing market more competitive, by offering new opportunities to businesses old and new. This should not be considered as a
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