Research

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Overview

Research and Development (R&D) is the very pulse of what we do at Geno. It’s a critical first step in developing a new drug in our industry. While others have different approaches, to us, R&D is a creative exercise undertaken in a systematic manner. We treat reliable science as our backbone for everything we do.

Once our remarkable team of scientists identifies an initial candidate drug, we commit to rigorous research to determine its therapeutic suitability. Researchers from diverse walks of life come to Geno to increase our stock of knowledge. This includes our search for new molecules, synthesis and modification of known molecules or some methods to increase production rates by adopting assorted techniques. Together, the whole team of Geno is out to achieve our mission to serve the very best to our consumers.

Formulation Research & Development

Formulation development is a practice that helps us accurately assess the optimal dosage form, composition and manufacturing route for our products. We make sure to spend enough time and resource on each drug to optimise the drug’s delivery performance and product stability.

A key area of product development, it can determine patentability, lifecycle and, ultimately, the success of a pharmaceutical product. This is why we make sure that our processes lead us to the best possible result for the success of any new drugs.

Our R&D engages formulation development in the making of tablets, capsules, liquids &semisolid dosage forms. We expressly integrate process validation, analytical method validation, analytical method development as well as stability testing in line with best practices. Our formulation development team is also involved in trouble-shooting activities and are sure to participate in investigations if any product discrepancies arise.

Analytical Research & Development

Analytical method development, validation, and transfer are essential elements of any pharmaceutical development program.

An effective analytical method development confirms that laboratory resources are optimized, while methods are aligned with each stage of drug development. We use high performance liquid chromatography for the qualitative and quantitative analysis of a drug for its accuracy.

Since analytical method development and validation play such a crucial role in drug discovery, development and manufacturing, we ensure we exercise the greatest care. A number of chromatographic parameters have been evaluated in order to optimize the analysis of method development in High-performance Liquid chromatography (HPLC).

The analytical method validation is essential for analytical method development and so our methods are tested extensively for specificity, linearity, accuracy, precision, range, detection limit, quantization limit, and robustness.

Logistics

Geno believes in partnerships that aren’t just profitable, but are also valuable.

This is why we make sure our vendors are thoroughly vetted so that we can have enduring relationships with each of them. All procured materials are tested as per our protocol and only that material which meets our standards is used for production.

Once production is completed, we test our product again for quality control. We comply fully with all industry standards and regulations for testing. To ensure our robust trade supply runs smoothly we have a number of stockists, distributors, and retailers across India.