02.21.26 -- Aseptic Contract Manufacturing Services

Find tailor-made solutions designed to deliver high-quality standards even when scaling up. Modularity enhances production efficiency, saves costs, and shortens time to market.

Effective CDMO audits require clear agendas, thorough preparation, and strong communication to ensure compliance, minimize disruptions, and build collaborative relationships that enhance quality and regulatory confidence.

Discover plungers that are made from the best-in-class elastomeric formulations. From start to finish, NovaPure® components have been designed and manufactured using QbD principles to mitigate risk.

We leverage our distinctive geographical location to ensure the safe delivery and administration of quality drug products (DP) to patients with minimal safety risks.

Continuous flow processing can be integrated into a broader strategy. By optimizing processes to reduce waste, companies can demonstrate their commitment to environmental stewardship and meet regulatory requirements.

Sterile fill-finish and device assembly capabilities span global sites, offering scalable solutions, analytical testing, and regulatory compliance for combination products and small-batch technical programs.

Our capabilities support the development and cGMP-compliant production of complex small-molecule active pharmaceutical ingredients (APIs), registered starting materials (RSMs), and advanced intermediates.

By leveraging Pfizer’s global expertise and in-depth understanding of the complexity involved in OSD manufacturing, we help identify solutions quickly if and when issues arise.

Foreign Trade Zones help businesses cut costs and improve efficiency by deferring or eliminating tariffs, streamlining imports, and enabling faster market access while maintaining flexibility for global distribution.

Late phase development requires a holistic development strategy driven by a well-defined target product profile. Here's an overview of the complex path to a successful product launch.

Ensure your products and materials maintain integrity through distribution with robust package validation testing. Explore comprehensive capabilities including simulation and aging tests.

Meeting stringent requirements for sterile fill/finish operations hinges on robust contamination control strategies, advanced isolator technology, and rigorous integrity testing to ensure patient safety.

See how a cutting-edge, multi-purpose isolator line delivers high-speed, precision fill/finish. This flexible technology supports a diverse range injectable therapies.