Newsletter | April 1, 2024

04.01.24 -- Understanding And Navigating Diverse Regulatory Environments


Webinar: De-Risking The Aseptic Drug-Filling Process And Optimizing Production

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.


Understanding And Navigating Diverse Regulatory Environments

Drug developers aspire to treat patients globally, but navigating diverse regulatory structures around the world gets tricky. These consultants offer a primer on the regulatory bodies of the world.


A Smart, Data-Driven Approach To Formulate Biotherapeutics For PFS

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.

The Bioanalytical Development Journey

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.

A Molecule’s Journey: Break Down Roadblocks To Clinical Success

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?

Getting Your Biologic To Clinic Faster And More Efficiently

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.

Revolutionizing Particle Characterization With Image Analysis And ML

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.

Plan Your CDMO Search On A Foundation For Long-Term Success

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


Your Trusted Partner Of Choice For Prefilled Syringe Success

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

OPTIMA 7000 Fill Line

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.

Combining Scientific Knowledge And Advanced Technology

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.


Find Your New CDMO At Outsourced Pharma Capacity Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capacities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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