"It was a wonderful experience interacting with you and appreciate the way you have planned and executed the whole publication process within the agreed timelines.”
Subrat SaurabhAuthor of Kuch Woh Pal
Quality assurance in the pharmaceutical industry encompasses rigorous standards and processes aimed at ensuring the safety, efficacy, and reliability of medicinal products. It involves implementing quality control measures, adhering to Good Manufacturing Practices (GMP), and embracing Total Quality Management (TQM) philosophies to foster continuous improvement. Regulatory guidelines, such as those outlined by the International Conference on Harmonization (ICH), play a pivotal role in standardizing practices and ensuring global alignment in quality standards. Moreover, initiatives like Quality by Design (QbD) emphasize proactive approaches to product development, emphasizing risk management and optimization throughout the manufacturing process. Adherence to international standards like ISO 9000 and ISO 14000, along with accreditation processes such as NABL, further solidify the commitment to quality excellence and regulatory compliance across all facets of pharmaceutical operations.
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Mrs. Dhruti Mehta, Dr. Ram Narayan Prajapati, Dr. Rajesh Sharma, Dr. Alankar Shrivastava, Dr. Pradeep Swarnkar
Dhruti Mehtais working as an Assistant professor, Geetanjali Institute of Pharmacy, Geetanjali University, Udaipur (Raj.). She is a dynamic professional with a background in Pharmaceutical Sciences and a passion for sustainable development. She has completed her B.Pharm and M.Pharm studies from Geetanjali Institute of Pharmacy. She also has Post Graduate Diploma in Applied Nutrition and Dietetics from Symboisis University of Distance Learning, Pune, Maharashtra.
