Featured Solutions

1. Over-Encapsulation/Blinded Study Materials 2/14/2025

   Over-encapsulation is a popular, cost-effective technique that involves the blinding of a solid dosage form into a capsule shell in order to eliminate bias from comparative clinical trials, while maintaining study integrity and efficacy. If the blinding of the material is not adequately done, clinical trial participants may be able to tell the difference between the real drug and the placebo, resulting in a biased trial and a loss on your investment.

2. Applications Of Liquid-Filled Capsules In Pharmaceutical Manufacturing 1/17/2025

   Liquid-filled, two-piece capsules offer several advantages over other solid dosage forms, such as ease of scalability and manufacturing, faster absorption, simpler packaging, and higher product stability. Liquid filling also offers the ability to control R&D compounds, which are expensive and in limited supply. They are also known to accelerate product development because they can be made with fewer excipients than other solid dosage forms, such as tablets. 

3. Wet Nanomilling And Vial Filling 9/9/2024

   Nanomilling revolutionizes drug delivery by reducing particle size to enhance solubility, bioavailability, and therapeutic efficacy, addressing the challenges of poorly water-soluble APIs.

4. Terminal Sterilization 7/18/2024

   There is a growing demand for the sterilization of small-molecule parenteral products, including heart medications, eye drops, analgesics, and antibiotics, as well as intravenous solutions, such as glucose, potassium, and saline. To ensure patient safety, these drug products and related instruments commonly used in hospitals must be thoroughly sterilized after being manufactured. Known as "terminal sterilization," this highly efficient process ensures that no microbial contaminants like fungi or bacteria are present when the product is used.

   If you have a product that needs to be terminally sterilized, we can help.

5. Pharmaceutical Formulation Development 6/7/2024

   Proper formulation of active pharmaceutical ingredients (APIs) is essential for achieving therapeutic efficacy, ensuring patient safety, maintaining product stability, optimizing pharmacokinetics, meeting regulatory requirements, and enhancing cost-effectiveness in pharmaceutical development.

6. Top Contract Drug Development And Manufacturing Company 5/8/2024

   Altasciences' manufacturing (CDMO) team provides tailored solutions for each phase of your drug development program. From discovery to market ― they’ve got you covered!

7. Comprehensive Services For Ophthalmic Drug Development 4/9/2024

   With our specialized support, you can be confident that your ophthalmic drug will not only meet regulatory standards but also address unmet medical needs in the most expedited manner possible.

8. Comprehensive Services CNS Drug Development 4/9/2024

   Our approach is designed to optimize efficiency and accelerate timelines, resulting in up to 40% time savings throughout the early phases of your drug development journey.

9. Your Top Partner For Ophthalmic Drug Development 4/9/2024

   As a leading partner in ocular therapy, Altasciences is at the forefront of ophthalmic drug development. Our integrated CRO/CDMO solutions can support your program from lead candidate selection to market. You will benefit from working with a single partner as your product advances through each phase of drug development—from prototype formulation through preclinical testing, to early phase clinical trials, and manufacturing. This could mean up to 40% in time savings.

10. Contract Drug Development, Manufacturing, And Analytical Testing 1/29/2024

    Explore our collection of capabilities, including liquid-filled capsules, band/sealing technologies, powder, over-encapsulated capsules, topical formulations, and clinical and blister packaging.