February 16, 2024
Root Cause Analysis with example for “5” Why technique
Root Cause Analysis (RCA) is a method that is used to address a problem or non-conformance in the quality process to get to the “root
See our latest Articles
February 6, 2024
Why is embracing the Document Management System still intimidating?
DMS in a layperson perception A thorough-cum-simpler explanation of Document Management System will make us understand about the efficacy of this digital trend. With the
February 6, 2024
Benefits of Training Management System
Here’s what a Training Management System can, and should, do for you: Learning Management System makes it very easy for trainers to update existing training
February 6, 2024
GAMP 5 Categories, V Model and 21 CFR Part 11, EU Annex 11
What is GAMP 5? Good Automated Manufacturing Practice, Founded in 1991. International Society for Pharmaceutical Engineering (ISPE) sets the guidelines for manufacturers and the current
February 6, 2024
Integration of Artificial Intelligence and Machine Learning in QMS
Integration of AI & ML in Quality Management Systems There is no doubt that we have entered the new industrial revolution, commonly referred to
February 6, 2024
Top 9 Challenges and Solutions for eDMS Software in Pharma Industry
The pharmaceutical industry operates in a highly regulated and complex environment, facing numerous challenges that can impact productivity, compliance, and overall efficiency. Managing documents from
February 6, 2024
AmpleLogic: Offering GMP Quality Management System to Achieve Optimum ROI
The aging population, chronic and lifestyle diseases, emerging-market expansion, and treatment and technology advances are expected to spur life sciences sector growth in 2015. Furthermore,
February 6, 2024
Remarkable height of digitalization in Pharma Businesses with DMS
Go Paperless with Document Management System Gone are the days when we used to keep all our essential information and crucial data in tones of
April 10, 2023
A Comprehensive Insight on Various Audit Types in Quality Management
Quality audits specifically examine how well product designs and processes meet specified standards and regulatory compliances. They are performed periodically by internal people within the
April 10, 2023
Revolutionizing Regulated Industries: Unleashing the Power of aPaaS with COTS and Low-Code Platforms
In the ever-evolving landscape of regulated industries such as life sciences, pharmaceutical manufacturing, gene therapy and medical devices; the demand for cutting-edge technology solutions is
April 10, 2023
8 Common GCP Violations in Clinical Trials
Clinical trials are crucial for advancing medical research, but ensuring their integrity and adherence to ethical guidelines is paramount. Good Clinical Practice (GCP) guidelines serve as the
April 10, 2023
Essential Elements of Enhancing Healthcare Quality: 5 Key Components
Most people believe cybersecurity is highly complicated, ever-changing, and technical. They’re not wrong.
April 10, 2023
Streamlining Pharmaceutical Manufacturing with DMS Software
Maintaining strict quality standards, efficient processes, and compliance with regulatory requirements is paramount in the highly regulated and complex pharmaceutical industry. Document control plays a
April 10, 2023
Achieving data integrity is made easy with eDMS in the pharmaceutical industry
Data integrity reaffirms the pharmaceutical industry’s commitment to manufacturing safe, effective drugs that satisfy quality standards. Simultaneously, data integrity is a vital tool for regulatory
April 10, 2023
Top 7 Queries Addressed: Data Integrity and CGMP Compliance
This article provides a clear insight into the significance of data integrity within the framework of current good manufacturing practice (CGMP) for pharmaceuticals, as mandated
April 10, 2023
Unveiling the 8 Benefits of Quality Management Software in Pharma
As manufacturers in the pharmaceutical industry face new-market demands, intricate supply chains, and evolving regulations, there is a growing need to reassess outdated and disconnected
April 10, 2023
Compliance with Schedule M of the Drugs and Cosmetics Act (2018)
In a recent announcement, Health Minister Mansukh Mandaviya emphasized the importance of complying with Schedule M of the Drugs and Cosmetics Act, prepared in 2018. A Pharma
April 7, 2023
7 Common Compliance Issues Faced by the Pharmaceutical Industry
The pharmaceutical industry is critical in safeguarding public health by researching, developing, and manufacturing life-saving drugs. However, this sector operates in a highly regulated environment
March 21, 2023
Pharma 4.0 Adoption in India: A Catalyst for Modernization in the Pharmaceutical
As the Indian pharma sector embraces digitalization and advanced technologies, several key transformations are expected: 1. Global Competitiveness: By going digital and incorporating Pharma 4.0, Indian
March 20, 2023
Are Your Logbooks in Place For The Upcoming Audit?
As a pharmaceutical manufacturer, you are likely familiar with the stringent regulatory requirements governing the industry. One critical aspect of compliance is o maintain accurate
March 20, 2023
8 Important KPI’s for Quality Management System
Key Performance Indicators (KPIs) are critical metrics that are used to measure the performance of a Quality Management System (QMS). They provide insight into how
March 20, 2023
Harmonizing Voluminous Logbooks eases Record Keeping in the Pharmaceutical Industry
The global pharmaceutical industry has boomed for decades by increasing its market in both the developed and the developing nation. With the evolution of data-
March 20, 2023
Implementing Time and Content Validation with Learning Management Software
The growing favour of e-learning through LMS Software earned friction across various businesses, particularly pharmaceutical firms. It’s one of the vital sectors in the European
March 20, 2023
Document Management Systems is a boon to the Topical Pharmaceutical Sectors
Incorporating new-age technology in Lifesciences: With digitalization in impact there has been a lot of astounding changes in every industrial sector including pharma and life
March 20, 2023
Tweaking V Model to Accelerate GMP Automation’s and Address Data Integrity Issues
A long list of data integrity warnings received by pharma companies has made them train their focus on building and fortifying their tracking mechanisms to
March 20, 2023
TOP 3 Trends Transforming Outlook of Pharmaceutical Industry In 2023
COVID-19 spurred a sense of urgency in healthcare and pharma professionals, making the entire landscape conducive to change and digital transformation. We’re at a strange
March 20, 2023
Pharma 4.0: Faster Digitalization with Low Code Platforms
Digitalization: An Evident Automation Revolution, Is automation a step-up for healthcare? Talking about digitalization will surely uncover a lot of facts, insights and statistics in
March 20, 2023
CSA (Computer Software Assurance) A move from Traditional CSV
Core to growing a gaming company is a robust payments infrastructure.
✔︎ Cyber Security
✔︎ Consulting services
March 18, 2023
Why growing Pharma Companies should automate their Quality Process
Automation Impacting Quality Process Quality Process Automation is not only the requirement of well-established pharma companies but also there is a huge demand and need for automation
March 18, 2023
Is the Learning Management System a new-age demand for digitalization today?
Traditional learning being powered up with LMS: If we talk about various achievements or success these days, we must have heard a lot about e-learning
