Featured Products

1. Flow Measurement 4/4/2012

   One for all - Endress+Hauser's multivariable metering. The ability to measure several process variables all at the same time opens up completely new application fields.

2. High-Performance Filtration For Optimal Life Science Workflows 9/26/2021

   Pall’s high-performance filtration solutions cover every step of the life science workflow - from cell line development to clone selection, optimization, and protein analysis. Our products simplify processes, reduce risk, and accelerate laboratory throughput.

3. Process Development 4/7/2020

   Our expertise in technology transfer and scale up ensures that the final product will be suitable for large scale manufacture and commercialization. We can provide small-scale proof of concept prototype batches, manufacture clinical trial materials; perform scale up manufacturing and registration batch manufacturing as well as perform product transfer and validation services in preparation for Commercial Manufacturing

4. Analytical Services 10/23/2024

   Upperton offers analytical services designed to support the development, monitoring, and quality control testing of pharmaceutical products.

5. Pharmaceutical Cleanroom Design Services 9/2/2020

   Your next cleanroom is more akin to a piece of equipment than a room. Operational efficiencies, compliant flow of materials and personnel, and lifecycle considerations should dictate the selection of your cleanroom partner. AES designers have been engineering functional cleanroom facilities for over three decades, guaranteeing the performance of each and every facility. Our in-house designers work as a team with our cleanroom construction personnel to engineer a cost-effective project while maximizing performance, value, and constructability. The greatest value is realized when AES is integrated into the design team at the start of the project. Early project integration with the AES experts helps the infrastructure team decide what support and cleanroom solutions the clean space requires. Early participation by AES saves design costs, expedites schedule, and eliminates a duplication of services.

6. 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.

7. Cleaning Validation (21 CFR Part 211.67) 12/5/2008
   Alconox, Inc. can assist you in selecting an appropriate cleaner for cleaning pharmaceutical manufacturing equipment and utensils to prevent malfunctions or contamination that would alter the safety, identity, strength, quality or purity of the drug product beyond the official or other established requirements.
8. Fully Integrated CDMO Services 6/22/2020

   Samsung Biologics is a reliable partner for seamless tech transfers, clinical and commercial manufacturing, aseptic fill/finish, and analytical testing. Committed to partnership, you will have a dedicated project management team walking you through your product’s entire development and manufacturing journey. We are committed to operational excellence in cGMP manufacturing and quality assurance.

9. Small Bottle Checkweigher: High-Accuracy Measurement For Small Containers 8/27/2024

   This checkweigher ensures stable transfer and high-accuracy measurement of small containers that can easily topple during conveyance, such as eye lotion bottles, nasal drop vials, and cosmetics containers. The model features a conveyor with three integrated side-grip belts that keep products upright throughout the infeed, weigh table, and outfeed sections. The width of these side-grip belts is easily adjustable to accommodate different product sizes, with a standard range of 20-40 mm and an optional maximum width extension up to 100 mm. This design allows for a processing speed of up to 200 bottles per minute and an accuracy of +/- 0.02 g. The rejector uses a gate-type mechanism, with an optional air jet rejector for products up to 200 g. The system is compliant with federal regulation 21 CFR Part 11 for the integrity of electronic records and signatures, with features such as password authentication, audit trail of operation data, and encryption/decryption of exported data.

10. Composable MES For Pharma 6/30/2025

    The Composable MES for Pharmaceuticals provides a starting point for you to implement a tailored, connected production system with end-to-end traceability and right-the-first-time electronic batch records (eBR).