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Subrat SaurabhAuthor of Kuch Woh Pal
Preformulation studies lay the groundwork for successful drug formulation by optimizing molecular properties, evaluating crystal morphology, and assessing powder flow. Understanding drug-excipient compatibility and employing methods like structure modification ensure the efficacy and stability of pharmaceutical products. In parallel, advances in formulation additives and excipient science facilitate innovative approaches to drug development, supported by techniques such as factorial design experiments for robust product and process optimization. Solubility and dissolution studies delve into crucial aspects of drug delivery, elucidating techniques like salt formation and solid dispersion to enhance bioavailability. Meanwhile, product stability assessments, including degradation kinetics and stability testing, adhere to stringent protocols and ICH guidelines to ensure quality and efficacy throughout a product's lifecycle.
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Mr. Ankur Agrawal, Mr. Chandan Kumar Raikwar, Dr. Masheer Ahmed Khan, Ms. Sameea Ahmed Khan, Dr. Rajesh Sharma
Mr. Ankur Agrawal is an esteemed Associate Professor at Jai Institute of Pharmaceutical Sciences and Research in Gwalior, Madhya Pradesh. His academic journey began with a B.Pharmacy from I.P.S College of Pharmacy, followed by an M.Pharm where he earned the distinction of being a Gold Medalist. Currently pursuing a Ph.D. in Pharmacy from ITM University, Gwalior, he is deeply immersed in advancing pharmaceutical education and research.
