Outsourced Pharma Products & Services

  1. Cell Line Development 2/17/2022

    Our experience developing mammalian and microbial cell lines and our analytical capabilities enable us to identify and select clones that meet your product’s specific parameters and characteristics.

  2. Comprehensive mRNA Solutions 1/31/2025

    Curia’s combined expertise and a proven track record of success in key scientific disciplines including molecular biology, protein production and analysis, enzymes, nucleosides and lipids is the foundation of our mRNA solution. Partner with us and harness our ability to provide high-quality constructs through in-house research and analysis capabilities that enable accelerated timelines for delivery.

  3. Small Molecule Process R&D And Manufacturing 5/16/2025

    Partner with us to deliver value-added scientific solutions — quickly, safely, and compliantly — with uncompromising quality.

  4. Speed to Study™ 8/3/2020

    As pharmaceutical companies seek to streamline early phase development to establish proof of concept quickly and efficiently, PCI’s Speed to StudyTM services are designed to manoeuvre complex trial designs with maximized flexibility and speed.

  5. Biologics Manufacturing 5/15/2024

    ReciBioPharm GMP manufacturing units focus on process robustness and consistency to ensure product quality, purity and efficacy. Our multi-product manufacturing facilities feature state-of-the-art equipment for animal cell-derived viral and microbial products for your clinical trials in phase 1-2 and in accordance with cGMP guidelines.

  6. Sterility Testing: An Essential Part Of Pharmaceutical Product Validation

    To effectively monitor product quality, it is critical to test for microbial contamination throughout the pharmaceutical manufacturing process. Sterility testing is a vital step to ensure products purporting to be sterile do not contain viable microorganisms prior to their distribution and administration to patients. Consequently, it is of utmost importance that the testing method employed for products, formulations, tissue materials, and medical devices is both accurate and reliable. Explore a collection of streamlined sterility testing solutions and expert guidance on sterility testing, quality control (QC), and data integrity. Optimize your sterility testing and QC procedures with world-leading tools and technologies that can help you ensure full traceability and regulatory compliance.

  7. Chain Of Compliance: Enabling A Significantly Smarter Supply Chain 12/1/2022

    Companies vying to be the first to market with breakthrough treatments have a great deal riding on the success of their efforts. Incorporating innovative processes, ethical considerations, assuring the safety and efficacy of the product, and managing the commodity's environmental control are formidable challenges that often lack standardized quality control procedures. Precision medicine requires end-to-end traceability: everything from chain of custody, to chain of condition, to chain of identity. The fragility of regenerative medicine therapies and the need to manage risk means a fourth link in the chain will soon be a regulatory requirement.

  8. Tablet Press Turrets 3/16/2009

    All Natoli turrets manufactured are designed to improve alignment and increase longevity.

  9. '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.

  10. GMP Manufacturing 4/24/2023

    Nanoform’s GMP facility utilizes its award-winning Controlled Expansion of Supercritical Solutions (CESS®) technology for the manufacture of API nanoparticles to GMP standards.