5 Ways Altasciences Can Help You Move Through the Early Drug Development Phases

1. 5 Ways Altasciences Can Help You Move Through the Early Drug Development Phases

2. 5 Ways Altasciences Can Help You Move Through the Early Drug Development Phases If your organization is ready to start drug development, you want a CRO with CDMO pharma capabilities on your side. Thankfully, Altasciences is prepared to be your partner and help you successfully develop your latest therapeutic drug. Since Altasciences is a fully integrated CRO/CDMO, information flows freely, potential roadblocks caused by using multiple CROs can be avoided, and your drug development cycle has a much higher chance of running smoothly. Here are a few of the ways Altasciences can help your organization as it moves through the early phases of drug development. Navigating Regulatory Approval If your organization has never submitted an Investigational New Drug application, the Altasciences team can help. The team has extensive experience navigating the murky waters of regulatory requirements. They keep up-to-date on the changing landscape as regulations evolve. The Altasciences team can help by preparing a study design that best accommodates your goals and specifications while still meeting regulations.

3. Designing Clinical Trials Has your team designed a first-in-human clinical trial before? If not, trust the Altasciences team for support. The Altasciences team can design and conduct clinical trials, leveraging the preclinical data to help you generate data to meet your objectives. Their team has access to essential resources and Phase 1 clinical trial units for overnight studies or necessary medical equipment. Recruiting Potential Participants The Altasciences team has full access to potential participants for your clinical trials. They will lead all recruiting efforts in-house, from determining the best types of advertising to reach your target demographic to conducting interviews and obtaining informed consent. The team also keeps a database of more than 400,000 potential participants, which can streamline the recruiting process. If you partner with Altasciences during early clinical development, the recruiting team can start the process early, ensuring participants are ready to go when it’s time for trials to begin. Manufacturing Therapeutic Drugs As a CRO/CDMO, Altasciences is capable of in-house production. This could mean producing drug capsules for the clinical trial or ramping up production to take your therapeutic drug to market. Thanks to their open communication style, information can be shared between teams and the manufacturing process is simplified and streamlined. Thanks to data collected during early clinical development, the manufacturing team will be ready, minimizing start-up time for manufacturing. Bioanalysis Capabilities Altasciences also offers a full range of bioanalysis expertise to their partners. The Altasciences team can process more than 60,000 samples per month using state-of-the-art, purpose-built laboratories. From small and large molecule bioanalytical services and microsampling, their unique array of platforms and an extensive list of validated assays help ensure effective methods for your program. Partner with Altasciences for your drug development cycle at https://www.altasciences.com/ Original Source: https://bit.ly/3st9x6Q