Q2 Solutions can help drive your discovery phase structure activity relationship (SAR) by optimizing for ADME properties, in parallel to your receptor binding potency and selectivity, for more rapid identification of high quality drug candidates.
Navigating the challenges of developing a biosimilar through clinical trials while meeting regulatory guidelines requires an experienced partner. Q2 Solutions offers tailored solutions that will help you make informed decisions and shape validated outcomes for your study, from research to commercialization.
Q2 Solutions’ bioanalytical experts can partner with you to develop assays that incorporate state-of-the-art instrumentation, rigorous quality control, and a logistics infrastructure to support large-scale, international studies.
With the increased globalization of clinical trials and development of biologics, the clinical supply chain can feel like uncharted territory.What if you were able to tap into the experience of thousands of clinical trials when designing your drug supply strategy? What if you could see different ideas in practice and understand what works and what doesn’t?
Our analytical and research services evaluate the performance of formulations using a whole range of advanced investigative testing procedures. They’re a hugely important part of our work, forming a valuable foundation for future developments and innovations.
At Sharp, we’re here to help you overcome development challenges, keep costs down and accelerate your time to market. We’ll work with you to develop a reliable formulation that gives optimal clinical outcomes and can be easily reproduced on a large scale, with excellent stability.
Increasingly elaborate international clinical trials demand a smart, streamlined approach and at Sharp we use interactive response technologies (IRT) to provide just that. They’re a powerful, practical tool for accelerating your product’s progress to launch and making the management of your trial much easier for everyone.
At Sharp, we work closely with you to build an in-depth understanding of your goals, challenges and requirements before we begin our state-of-the-art manufacturing process. This enables us to tailor our clinical manufacturing services to meet your specific needs, making sure we deliver your product on time, to your exact specification, and all ready for a successful launch.
Whether you’re looking for a placebo to match your product or designing your trial dose to match an existing comparator, getting a good match can be almost impossible. That’s where we come in.
We can over-encapsulate solid oral dosage forms like tablets or capsules, backfill them with a suitable excipient and manufacture a placebo to match. This gives real scientific credibility to your clinical trial, maintaining the integrity of your double-blind study design.
At Sharp, we know that clinical studies are growing in complexity, with new geographic regions being introduced and fresh pressures on schedules, budgets and controls. That’s why our clinical packaging team does so much more than simply putting tablets in bottles.
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