Close
CDMO Safety Testing 2026
Novotech

Catalent Adds Potent Manufacturing Capabilities at its Buenos Aires, Argentina Site

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

โ€“ Access the Media Pack Now

โ€“ Book a Conference Call

โ€“ Leave Message for Us to Get Back

Related stories

SK Bioscience Inks Colombia Vaccine Localization Deal

In a critical step for Colombia vaccine localization, SK...

Choosing Analytical Instruments for Pharma QC Labs

Selecting the right laboratory equipment is a critical decision that directly impacts the efficiency, accuracy, and compliance of pharmaceutical operations. Evaluating analytical instruments pharma QC requirements involves a deep dive into technical specifications, vendor reliability, and the potential for long-term scalability. By choosing tools that integrate seamlessly with existing digital workflows and international regulatory standards, laboratory managers can ensure that their facility is equipped to handle the rigorous demands of modern drug testing and quality assurance. This strategic approach minimizes operational risk and ensures the delivery of safe and effective medications to patients globally.

Spectrophotometers Driving Accuracy in Drug Quality

Precision in pharmaceutical analysis is fundamental to ensuring that every therapeutic agent delivered to a patient meets the highest safety and efficacy standards. The implementation of high-grade spectrophotometers drug quality control workflows provides a scientific basis for quantifying chemical properties and physical characteristics with unmatched reliability. By leveraging advanced spectral data, manufacturers can validate formulations and detect impurities early in the production cycle, thereby reinforcing the integrity of the global supply chain, ensuring regulatory compliance, and protecting the well-being of patients around the world.
- Advertisement -

Catalent, the leading global provider of advanced delivery technologies, development, and manufacturing, solutions for drugs, biologics, cell and gene therapies, and consumer health products, announced that it will expand its Argentinian site in Loma Hermosa, Buenos Aires. The expansion, which will add over 11,000 square feet of production space at the facility, will be segregated and designed to handle cytotoxic and highly active products for prescription softgel manufacturing.

The new facilities, which are due to be completed in December 2021, will include two new manufacturing vessels of 40 and 300 liters, which include an automatic cleaning system and an innovative mixing device suitable for very high viscosity formulations, a capsule filling line and six drying tunnels. This will add a capacity of over 10 million doses per annum to the site, which supplies products to the Latin American, U.S. and European markets.

โ€œThis investment will allow the site to grow and handle a wider range of projects, reacting to the increased demands of the industry for high potency treatments in areas such as oncology,โ€ commented Sergio Alter, Vice President & General Manager Softgel Technologies, Latin America. He added, โ€œNot only will this increase the capacity of the site, but the design of the new facility will see it meet the highest standards of environmental and energy efficiency.โ€

Catalentโ€™s 265,000 square-foot-facility in Buenos Aires currently houses softgel manufacturing operations, providing customers with a full range of development services, from formulation to packaging.

ABOUT CATALENT

Catalent is the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, cell and gene therapies, and consumer health products. With over 85 years serving the industry, Catalent has proven expertise in bringing more customer products to market faster, enhancing product performance and ensuring reliable global clinical and commercial product supply. Catalent employs over 13,500 people, including approximately 2,400 scientists and technicians, at more than 40 facilities, and in fiscal year 2019 generated over $2.5 billion in annual revenue. Catalent is headquartered in Somerset, New Jersey.

Never miss a pharmaceutical headline

The pharmaceutical industry moves fast โ€“ stay on top of it with our must - read briefings.

  • The top pharma and life sciences stories, straight to your inbox
  • The biggest news, features, interviews, and analysis
  • Dedicated coverage of the key developments driving the global pharmaceutical sector

Latest stories

Related stories

SK Bioscience Inks Colombia Vaccine Localization Deal

In a critical step for Colombia vaccine localization, SK...

Choosing Analytical Instruments for Pharma QC Labs

Selecting the right laboratory equipment is a critical decision that directly impacts the efficiency, accuracy, and compliance of pharmaceutical operations. Evaluating analytical instruments pharma QC requirements involves a deep dive into technical specifications, vendor reliability, and the potential for long-term scalability. By choosing tools that integrate seamlessly with existing digital workflows and international regulatory standards, laboratory managers can ensure that their facility is equipped to handle the rigorous demands of modern drug testing and quality assurance. This strategic approach minimizes operational risk and ensures the delivery of safe and effective medications to patients globally.

Spectrophotometers Driving Accuracy in Drug Quality

Precision in pharmaceutical analysis is fundamental to ensuring that every therapeutic agent delivered to a patient meets the highest safety and efficacy standards. The implementation of high-grade spectrophotometers drug quality control workflows provides a scientific basis for quantifying chemical properties and physical characteristics with unmatched reliability. By leveraging advanced spectral data, manufacturers can validate formulations and detect impurities early in the production cycle, thereby reinforcing the integrity of the global supply chain, ensuring regulatory compliance, and protecting the well-being of patients around the world.

Bristol Myers Squibb Integrates AI to Advance Manufacturing Quality Systems

Bristol Myers Squibb has entered into a strategic agreement...

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

โ€“ Access theMedia Pack Now

โ€“ Book a Conference Call

โ€“ Leave Message for Us to Get Back

Translate ยป