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Drug Dissolution Services
11 services found
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Method Development and Method Validation for Particle Size: The size, distribution and shape of the particle size will affect the quality of drugs, such as dissolution, bioavailability, content uniformity and stability, and ultimately affect the safety, effectiveness and quality control of drugs. In the whole life cycle of drug ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Industry estimates indicate that over 80% of new chemical entities exhibit low solubility, low bioavailability, and/or low or inconsistent dissolution rates. Effectively addressing these drug solubility, bioavailability, and dissolution rate issues is critical to advancing compound development and providing patients with the therapeutic benefits ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Industry estimates indicate that over 80% of new chemical entities exhibit low solubility, low bioavailability, and/or low or inconsistent dissolution rates. Effectively addressing these drug solubility, bioavailability, and dissolution rate issues is critical to advancing compound development and providing patients with the therapeutic benefits ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Long-acting Controlled-release Injection Technologies: CD Formulation can provide our clients with long-acting formulation technologies. Our pharmacologists can provide strategies to extend the duration of action of a drug after injection by (1) modifying the drug structure to extend the half-life of the drug's degradation in the body, (2) ...
by:Broughton Laboratories based inNorth Yorkshire, UNITED KINGDOM
We have extensive experience in validating analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method validation activity to meet your requirements. This includes project planning, protocol writing, execution, statistical evaluation and final validation report writing to satisfy ...
by:Broughton Laboratories based inNorth Yorkshire, UNITED KINGDOM
We have extensive experience in developing analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method development activity to meet your requirements. This includes project planning, protocol writing, execution, and final development reports to satisfy your regulatory ...
by:Ardena Holding NV based inMariakerke, BELGIUM
At Ardena, we guide our customers into making smarter formulation choices. Ultimately, this reduces the risk of clinical failure and ensures your product reaches the clinic rapidly via the most efficient route. Solving a problem and saving time Overcoming development challenges is our speciality. We work with customers to understand their product needs and develop the best possible formulation. ...
Manufactured by:Ascendia Pharmaceuticals based inNorth Brunswick, NEW JERSEY (USA)
Nanotechnology is now being extensively utilized in the development of innovative drug delivery systems for various routes of administration. Due to the advantages of their targeted drug delivery, reduced toxicity, long circulation, and enhanced half-life, nanoparticles are particularly useful for use in long acting formulations. Different types of injectable nanomedicines have been ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
In Vitro Dissolution Assay: The dissolution rate test of the drug was determined using an in vitro dissolution assay. For poorly soluble drugs and their oral dosage forms, such as tablets, capsules and suspensions, the dissolution of the drug in the body fluids at the absorption ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
The dissolution rate test of the drug was determined using an in vitro dissolution assay. For poorly soluble drugs and their oral dosage forms, such as tablets, capsules and suspensions, the dissolution of the drug in the body fluids at the absorption site is the rate-limiting step in ...
Manufactured by:Avantor, Inc. based inRadnor, PENNSYLVANIA (USA)
As labs are increasingly expected to maximize lab output while increasing ROI, many have embraced the role of on- and off-site dedicated scientific service partners as a means of generating new value streams within work models. Avantor’s teams of degree-level chemists, biologists, and engineers create your extended support team, performing protocol-driven work and implementing efficiencies ...