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The Future of Laboratory Automation with LIMS
Introduction A Laboratory Information Management System (LIMS) is an essential software solution used to automate the day-to-day...

companyconnectc
May 1, 202510 min read


21 CFR Part 11 Explained: A Complete Guide to FDA Electronic Records Compliance
Introduction 21 CFR Part 11 is necessary to guarantee the integrity, reliability, and security of electronic records and signatures in...

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Apr 26, 20253 min read


The Future of Drug Regulatory Affairs: Trends to Watch in 2025 and Beyond
Introduction The drug regulatory affairs function is an integral component of guaranteeing that pharmaceutical products are of the...

companyconnectc
Apr 19, 202510 min read


Common Pitfalls in CSV and How to Avoid Them
Introduction Briefly explain the significance of CSV (Comma-Separated Values) format in data handling. The CSV (Comma-Separated Values)...

companyconnectc
Apr 17, 202521 min read


Why CSV is Critical in the Pharmaceutical and Life Sciences Industries
Introduction Overview of the significance of data management in the pharmaceutical and life sciences sectors. In the pharmaceutical and...

companyconnectc
Apr 16, 202512 min read


How Personalized Medicine is Shaping Regulatory Frameworks
Introduction Personalized medicine, or precision medicine, is a fast-evolving field of healthcare that personalizes medical care...

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Apr 12, 202510 min read


Difference Between Computer System Validation and Software Testing
Introduction Explanation of Continuous Validation (CV) and its relevance in the context of Computer System Validation (CSV). Continuous...

companyconnectc
Apr 10, 202519 min read


The Future of Pharma Regulatory Affairs: Trends to Watch in 2025
Introduction to Regulatory Affairs in Pharma Regulatory affairs is a key activity in the pharmaceutical sector, confirming that medicines...

companyconnectc
Apr 7, 20257 min read


Global Regulatory Harmonization: Progress and Challenges
Introduction Global regulatory harmonization is of paramount importance in the pharmaceutical and biotechnology sectors, with the...

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Apr 6, 20257 min read


Digital Health Products & Regulatory Pathways
Introduction Digital health products encompass a wide range of technology-driven solutions designed to enhance healthcare delivery,...

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Apr 2, 20256 min read


Continuous Validation: Is It the Future of CSV?
Introduction Explanation of Continuous Validation (CV) and its relevance in the context of Computer System Validation (CSV). Continuous...

companyconnectc
Mar 31, 202519 min read


India's Evolving Drug Regulatory Landscape: CDSCO Updates
Introduction to CDSCO Overview of the Central Drugs Standard Control Organization (CDSCO) The Central Drugs Standard Control Organization...

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Mar 29, 20258 min read


How to Conduct a Computer System Periodic Review
Introduction Importance of conducting a periodic review. Importance of Conducting a Periodic Review in Computerized System Validation A...

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Mar 28, 202513 min read


How to Build a Compliant Validation Plan
Introduction Importance of a compliant validation plan in regulated industries. In regulated industries such as pharmaceuticals,...

companyconnectc
Mar 27, 202517 min read


The Role of Artificial Intelligence in Accelerating Drug Discovery and Development
Introduction The drug discovery and development process is a complex and multi-stage journey that involves the identification of new...

companyconnectc
Mar 27, 202512 min read


The Role of Blockchain in Drug Supply Chain Integrity and Regulatory Compliance
Introduction Ensuring the integrity of the drug supply chain is crucial to safeguarding public health and ensuring that patients receive...

companyconnectc
Mar 26, 20258 min read


The Impact of Cloud-Based Systems on CSV
Introduction Overview of CSV (Comma-Separated Values) and its traditional use in data handling. Comma-Separated Values (CSV) is a widely...

companyconnectc
Mar 24, 202520 min read


Regulatory Affairs Career Roadmap: Skills in Demand for 2025
Introduction Regulatory Affairs is a critical function within the pharmaceutical and biotechnology industries , acting as the bridge...

companyconnectc
Mar 23, 20258 min read
How to Build a Compliant Validation Plan
Introduction Importance of a compliant validation plan in regulated industries. In regulated industries such as pharmaceuticals,...

companyconnectc
Mar 22, 202517 min read


Sustainability and Green Chemistry in Drug Development
Introduction The pharmaceutical industry is essential for global healthcare, yet its environmental impact has become a growing concern....

companyconnectc
Mar 19, 20255 min read
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