Summer Internship

I had the opportunity of working with formulation, quality, microbiology, analytical and the market research team at this company. This gave me a thorough walk-through of a medical product development. I assisted with various techniques and processes as listed below and finally submitted an extensive report on my experience at Piramal.

The process of formulating a herbal baby hair shampoo involved a comprehensive study and analysis of various components to create an effective and safe product tailored for infant use. Various extract phases, oils, and shampoo bases were meticulously examined and assessed to determine their compatibility and benefits for baby hair care.

By conducting thorough market research, the optimal proportions of each ingredient were identified. This research involved assessing existing baby hair care products, analyzing customer preferences, and studying the specific needs of baby hair and skin. The proportions of the extract phases, oils, and shampoo bases were carefully balanced to ensure both cleansing efficacy and gentleness, taking into consideration factors such as potential irritants and allergens.

The implementation of Quality Control (QC) for drug formulations is a vital step to ensure the safety, efficacy, and consistency of pharmaceutical products. In this context, a range of sophisticated techniques were employed to assess the quality and characteristics of the the product formulations, focusing on both chemical and physical aspects.

Biochemical assays and an array of tests were carried out, utilizing techniques such as High-Performance Liquid Chromatography (HPLC), High-Performance Thin-Layer Chromatography (HPTLC), and fingerprinting profiles of capsules. These techniques allow for the identification and quantification of specific compounds, ensuring that the intended active ingredients are present in the correct amounts.

Further analyses, such as disintegration time tests for capsules, ash tests, and microbiological analysis, were conducted in accordance with established standards like the US Pharmacopeia (USP) and British Pharmacopeia (BP). These tests assess parameters like disintegration, residue content, and microbial contamination, ensuring that the drug formulations meet stringent quality and safety standards.

Overall, the implementation of Quality Control through a diverse array of tests and techniques ensures that the drug formulations are consistent, safe, and effective. This rigorous quality assessment is essential to building trust among healthcare professionals and consumers, assuring them that the products they are using adhere to the highest industry standards.