Drug Formulation and All Dosage Forms

Our drug formulation service focuses on developing precise and effective formulations that adhere to global regulatory standards. We carry out extensive testing on all dosage forms including tablets, capsules, syrups, and injections, ensuring that they deliver consistent results every time. From the initial research phase to the final product, we monitor every stage to guarantee the formulation’s quality, safety, and efficacy. This process helps in creating pharmaceutical products that are not only safe for patients but also highly reliable in their intended use. We understand that each drug formulation must be tailored to meet the specific needs of patients and the demands of the pharmaceutical market. That’s why we apply cutting-edge technology and stringent quality control measures to ensure that every product produced is of the highest standard. Whether it’s a novel drug or a generic product, our thorough testing guarantees optimal performance, stability, and compliance with international quality standards.

API and Excipients

Active Pharmaceutical Ingredients (APIs) and excipients are the backbone of drug production, and we ensure their highest quality and compliance with regulatory standards. Our rigorous testing process ensures that APIs meet purity and potency specifications, and that excipients maintain their functionality without compromising the overall drug performance. By evaluating these crucial components, we ensure that each drug formulation is reliable, effective, and safe for use. We meticulously analyze these substances to ensure they meet all safety and regulatory requirements before they are incorporated into any pharmaceutical product. Our expert team provides thorough testing services for both APIs and excipients, evaluating their stability, composition, and compatibility within a formulation. By doing so, we help manufacturers streamline production while ensuring regulatory compliance and product safety. We offer customized solutions to address specific needs, whether it’s improving the efficacy of an API or ensuring the right excipient is chosen for the desired dosage form. Our focus on quality and precision helps pharmaceutical companies stay ahead in an ever-evolving market.

Analytical Method Validation

Our analytical method validation services are designed to ensure the accuracy, precision, and reliability of testing processes used in pharmaceutical and chemical industries. We develop and validate analytical methods that provide precise results, ensuring compliance with global regulatory standards such as GMP and ICH. Whether it’s for drug testing, stability studies, or raw material analysis, our validated methods ensure consistent and reproducible results that are critical for product quality and regulatory submissions. With our extensive experience in method validation, we offer solutions that guarantee the integrity of your product throughout the development and manufacturing process. From HPLC to spectroscopy, we employ a range of advanced techniques to validate methods across a variety of testing protocols. Our validated methods help pharmaceutical companies demonstrate compliance, ensure the reliability of their products, and streamline regulatory approvals, ensuring that only the highest quality products reach the market.