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Most small molecule drugs are formulated as oral solid dosage (OSD) forms, such as tablets or capsules. OSD has been an important part of the global pharmaceutical market. The formulation team of Crystal Pharmatech is formed by technical experts with considerable experience in formulation development and dosage form optimization. We design and develop the solid dosage form and process tailor-made for your molecule based on a deep understanding of the material properties of API and to meet its intended clinical needs.

The number of people with diabetes rose from 151 million in 2000 to 463 million in 2019; by 2045 this number will rise to 700 million. 1 in 5 of the people who are above 65 years old have diabetes, 1 in 2 people (232 million) with diabetes were undiagnosed, and diabetes caused 4.2 million deaths. Diabetes caused at least USD760 billion dollars in health expenditure in 2019 - 10% of total spending on adults. More than 1.1 million children and adolescents are living with type 1 diabetes, and 374 million people are at increased risk of developing type 2 diabetes.

A pioneer in dental treatment in Chennai and one of the best dental clinic in Chennai. The state of the art dental clinic in Chennai, offering sophisticated dental service in Chennai.

Deosen Biochemical (Ordos) Ltd. is a national high-tech enterprise who is specializing in the R&D, production, sales, and technical services of hydrocolloids and stabilizers. Deosen was established on July 3rd, 2005. It originated from Shandong Zhongxuan Corporation Ltd. which was founded in 1992. Now Deosen's production base is headquartered in Ordos City, Inner Mongolia, and the sales department is headquartered in Zibo City, Shandong Province.

We will provide our valued customers with analytical chemistry testing research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing. Analytical Method Development and Validation Guided by Quality by Design (QbD), we provide comprehensive analytical method development and validation in accordance with ICH Q2 based on Critical Quality Attributes (CQA) to support oral dosage form development. We also perform life cycle management to ensure quality research and control and provide accurate and reliable data at different drug development stages.

We will provide our valued customers with analytical chemistry testing services research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing. Analytical Method Development and Validation Guided by Quality by Design (QbD), we provide comprehensive analytical method development and validation in accordance with ICH Q2 based on Critical Quality Attributes (CQA) to support oral dosage form development. We also perform life cycle management to ensure quality research and control and provide accurate and reliable data at different drug development stages.

Bioavailability Enhancement for Insoluble Compounds & PROTAC & Oral Peptides Recent statistics indicate that approximately 40% of currently marketed drugs and nearly 90% of candidates in R&D pipeline belong to Biopharmaceutics Classification System (BCS) II or IV poorly water-soluble drugs. Consequently, enhancing drug solubility and improving bioavailability are pressing challenges in the realm of new drug development. Widely employed methods for solubility enhancement include: