We offer pharmaceutical development services including formulation, scale-up synthesis, stability testing, and forced degradation studies. Our team ensures your API or formulation meets global quality, regulatory, and stability requirements from R&D to commercial manufacturing.
IntroductionStability studies are a cornerstone of pharmaceutical product development. They evaluate how environmental factors like temperature, humidity, and light affect the quality of a drug over time. These studies help... Read more
IntroductionScale-up synthesis is the crucial process of transitioning a chemical synthesis route from the laboratory to pilot or full-scale manufacturing. It ensures that the Active Pharmaceutical Ingredient (API) or intermediate... Read more
IntroductionFormulation development is the science of designing and optimizing a drug product’s composition to ensure therapeutic effectiveness, safety, and patient compliance. Whether it's a tablet, injectable, cream, or capsule, every... Read more
IntroductionForced degradation studies are an essential part of pharmaceutical development, providing insight into the stability and shelf life of active pharmaceutical ingredients (APIs) and drug products. These studies simulate extreme... Read more