About Velesco pharmaceutical services
Velesco Pharmaceutical Services: Your Trusted Partner in Analytical Drug Development, Formulation, and GMP Manufacturing
Velesco Pharmaceutical Services is a Contract Development and Manufacturing Organization (CDMO) that specializes in analytical drug development, drug formulation, and Good Manufacturing Practice (GMP) manufacturing. With over a decade of experience in the pharmaceutical industry, Velesco has established itself as a trusted partner for companies looking to bring their drugs to market.
Analytical Drug Development
At Velesco, we understand the importance of analytical testing throughout the drug development process. Our team of experienced scientists uses state-of-the-art equipment and techniques to provide accurate and reliable data on your drug substance or product. We offer a wide range of analytical services including method development and validation, stability testing, impurity identification and characterization, extractables/leachables studies, particle size analysis, among others.
Drug Formulation
Formulating a drug product requires expertise in both science and art. At Velesco we have both. Our team of formulation scientists has extensive experience developing formulations for various dosage forms including tablets/capsules/sachets/powders/liquids/topicals/injectables/nasals/buccals/sublinguals/transdermals etc., with different release profiles such as immediate release/modified release/delayed release/targeted delivery etc., using different technologies such as granulation/coating/hot melt extrusion/spray drying/microencapsulation/nanoemulsion etc.
We work closely with our clients to develop formulations that meet their specific needs while ensuring regulatory compliance. We also offer pre-formulation studies such as solubility/permeability/dissolution/enzyme stability studies to help select the best candidate for further development.
GMP Manufacturing
Once your drug product is ready for clinical trials or commercialization you need a reliable partner who can manufacture it under GMP conditions. At Velesco we have an FDA-inspected cGMP facility equipped with modern equipment capable of producing batches from grams to kilograms scale using various technologies such as wet granulation/dry granulation/tablet compression/capsule filling/liquid filling/topical cream/gel/lotion manufacturing/injectable vial/filling/sealing/labelling/packaging etc.
Our Quality Assurance team ensures that every batch meets all applicable regulatory requirements before releasing it for use or distribution.
Why Choose Velesco?
At Velesco Pharmaceutical Services we are committed to providing our clients with high-quality services at competitive prices while maintaining strict confidentiality throughout the project lifecycle. We pride ourselves on being flexible enough to accommodate our client's changing needs while delivering projects on time without compromising quality or safety.
Our experienced team includes Ph.D.-level scientists who have worked in academia/pharmaceutical industry/regulatory agencies; thus they bring diverse perspectives which help us solve complex problems efficiently by applying scientific principles creatively.
We also offer project management services where one point-of-contact will be assigned who will coordinate all aspects of your project from start-to-finish so that you can focus on other important aspects like fundraising/marketing/business development etc., without worrying about technical details.
Conclusion:
If you are looking for an experienced CDMO partner who can help you navigate through the complex world of pharmaceutical development then look no further than Velesco Pharmaceutical Services! Contact us today to learn more about how we can help bring your drugs from concept-to-commercialization faster!
velescopharma.com