04.01.24 -- Understanding And Navigating Diverse Regulatory Environments

In the aseptic drug-filling process for biotherapeutics, your company may find it challenging to meet regulatory compliance standards, putting the safety and effectiveness of your products at risk. Join us and gain valuable insights into enhancing the efficiency and reliability of the drug product manufacturing process. Learn innovative strategies and best practices from industry experts to refine your pharmaceutical production methods. Click here to learn more.

Review technical considerations and case studies for how a partnership may help to overcome some of the challenges associated with selecting the optimum biotherapeutic presentation and PFS combination.

Learn how a CDMO with the capability to develop assays to support a wide range of drug substances can support your journey from discovery to clinical manufacturing with reduced cost and time.

The key to a biopharma executive's success is making the right decisions at the right time. Which will get your biologic to the clinic quickly and cost-effectively, without compromising quality and patient safety?

There are a range of benefits from using an integrated supplier to streamline biologic drug development starting in early phase through clinical and commercial stages.

The biopharmaceutical industry is increasingly employing micro-flow imaging for particle characterization, owing to the superior insights it can afford into product quality and process controls.

Capacity constraints typically are accompanied by other challenges, including missed timelines, defect rates, and overall decreased satisfaction with pharma companies’ bioprocessing CDMOs.

Prefilled syringes have become an increasingly attractive choice for medical professionals. Explore an optimized experience in the development and commercial manufacture of prefilled syringes.

We are a leader in aseptic filling, offering a wide range of capabilities for vials with our OPTIMA 7000 fill line. The OPTIMA VFVM 7000 safely processes various types and classes of biopharmaceutical products in 2 mL to 100 mL sizes.

We are your partner in contract production and development using the end-to-end business model. We specialize in the production of sterile biotechnological products in a manufacturing plant that meets the requirements of GMP.