Outsourced Pharma Products & Services

  1. Analytical Method Development And Validation 7/29/2024

    In pharmaceutical testing, the development and validation of analytical methods are absolute musts when it comes to reliable quality control. Natoli Scientific is at the forefront of offering comprehensive analytical method development and validation services designed to ensure the integrity of your company’s drug formulations. Our expert team develops robust methods tailored for each unique compound, with an approach that emphasizes precision, accuracy, sustainability, and compliance with regulatory standards such as the FDA and ICH guidelines. These methods are meticulously validated to confirm their reliability across a range of analytical parameters including specificity, sensitivity, linearity, and reproducibility.

    This validation process is critical for verifying that our methods produce consistent, trustworthy results throughout the product’s lifecycle, thus fostering confidence in the safety and efficacy of pharmaceutical products.

  2. Pharmaceutical Quality Management System (QMS) Software 2/7/2023

    Managing documents, training, and business processes are nightmares shared by all pharmaceutical and biotech companies and MasterControl provides pharmaceutical quality management software systems to take them out from that nightmare. MasterControl's QMS software exchanges the nightmares for a dream of a solution that enables pharma companies get their products to market faster and improve compliance at the same time. MasterControl pharma QMS software has been specifically designed to help manage all documents and automate regulatory-related processes and training in a single platform.

  3. 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.

  4. Pharmaceutical Packaging Design And Development Services 8/3/2020

    PCI’s pharmaceutical packaging design department provides an innovative and value added service. Our dedicated team of in-house design specialists deliver insightful packaging design and practical knowledge to deliver differentiated and cost-effective packaging solutions.

  5. Continuous Flow Processing 9/26/2024

    Continuous flow processing can be integrated into a broader strategy of sustainable manufacturing. By optimizing processes to reduce waste, energy consumption, and environmental impact, pharmaceutical companies can demonstrate their commitment to environmental stewardship and meet regulatory requirements for sustainable practices.

  6. 'B' Tooling Storage Boxes 1/20/2010

    Tooling storage boxes safely store and protect punches and dies. They are constructed of easy-to-clean, FDA-approved materials. Each box contains an easy lift-out tray and nested lid for stacking.

  7. Ion Exchangers: Capto™ S, Capto Q, & Capto DEAE 10/17/2011

    Capto S, Capto Q and Capto DEAE are, respectively, strong cation, strong anion and weak anion exchange media for packed bed chromatography that increase speed and throughput in capture and intermediate purification.

  8. Viral & Gene Therapy Manufacturing CDMO Services 6/15/2021

    You’ve developed your viral vector gene therapy and now it’s time to embark on the voyage to manufacturing. But gene therapy production is uncharted territory, and you need someone to help navigate through the process. We can help.

  9. Microbial Expertise 9/30/2024

    This content was created by Boehringer Ingelheim BioXcellence™

    Microbial product market is a market with attractive growth – and that growth is coming from diverse molecule formats and process formats where Boehringer Ingelheim in Vienna has outstanding development and manufacturing experience. We’re proud to be pioneers in the microbial field, with a track record of success going back to the 1980s and our work on recombinant interferons. Since then, we have brought 20 microbial manufactured products to the global market: some our own, some as trusted manufacturing partner.

  10. 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!