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How Altasciences Can Help Your Clinical Trials Stay on Schedule

When performing early-phase development of a new pharmaceutical drug, you need a contract research organization that can help you stay on schedule. Altasciences can help streamline your entire process, from preclinical to clinical proof of concept, and beyond. As an integrated CRO and pharmaceutical CDMO, Altasciences can also turn your clinically tested drug into a finished product. Here are three ways Altasciences can help keep you on schedule.

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How Altasciences Can Help Your Clinical Trials Stay on Schedule

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  1. How Altasciences Can Help Your Clinical Trials Stay on Schedule How Altasciences Can Help Your Clinical Trials Stay on Schedule

  2. How Altasciences Can Help Your Clinical Trials Stay How Altasciences Can Help Your Clinical Trials Stay on Schedule on Schedule When you need a contract research organization (CRO) and drug development solution that helps you stay on schedule, look no further than Altasciences. They know how frustrating delays and schedule changes can be during the drug development process. That is why they provide Proactive Drug Development. This integrated approach to early phase drug development can help reduce your program duration. Altasciences offers a full-service platform and customized processes to help you transition from one phase to another as smoothly as possible. Altasciences can help your program go smoothly with expertise in preclinical studies and CDMO pharma CDMO pharma solutions. Here’s how this integrated CRO/CDMO can help your drug development stays on schedule. Quick Access to NHP Studies Quick Access to NHP Studies Non-human primate (NHP) studies are a crucial preclinical step in drug research. Delays in NHP studies can last up to twelve months when it’s your next step for CNS clinical trials trials and other types of drug development. However, Altasciences can initiate studies in as little as three months with their steady supply of NHPs. Instead of relying on a single-source NHP supply, Altasciences diversifies their supply with a continuously maintained and backfilled population. With Altasciences, you can avoid these common delays and complete important steps on time. Thorough and Safety Thorough and Safety- -Oriented Precli Oriented Preclinical Drug Development Solutions nical Drug Development Solutions Altasciences has developed a preclinical drug development process that prioritizes your needs and the safety of your drug in a timely manner. Their integrated drug development solutions can help you reach essential decision-making milestones CNS clinical

  3. sooner. They perform a full range of in vivo non-GLP and GLP preclinical evaluations that can help assess the safety profile of both your large and small molecules. The Altasciences team has been conducting toxicology studies for decades and, therefore, can help make it easier for you to reach your targets on schedule. CDMO Pharmaceutical Solutions to Help Simplify Drug Development CDMO Pharmaceutical Solutions to Help Simplify Drug Development Altasciences is dedicated to being the contract development and manufacturing company (CDMO) that provides everything you need. As a pharmaceutical CDMO Altasciences can create a finished product of your clinically tested drug. They simplify the drug development process by being an attentive partner throughout the journey, from formulation all the way through commercialization. They offer a wide range of services, from nanomilling and grade C injectable drug processing to licensing and registrations. Altasciences performs all their production in their purpose-built facility equipped with devices to monitor temperature, humidity, and pressure. You can trust that the entire process will be handled by experts who can deliver your product on schedule. Keep your early phase drug development on schedule by partnering with Altasciences at https://www.altasciences.com/ https://www.altasciences.com/ Original Source: https://bit.ly/38xq4PV pharmaceutical CDMO,

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