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101 East Kennedy Boulevard, 41st Floor, Bank of American Plaza, Tampa, FL, 33602, US
Catalent is a leading CDMO championing the missions that help people live better and healthier lives. Catalent provides unparalleled service to pharma, biotech and consumer health customers, delivering on their missions to transform lives. Catalent tailors end-to-end solutions to meet customers’ needs in all phases of development and manufacturing.
When a biologic drug is being studied in a clinical trial, the sponsor may want to compare the investigational product to a current standard of care, known as a comparator drug. In other cases, a co-medication may need to be dosed along with the study drug. Sourcing commercially available branded biologics can be challenging for […]
Released By Catalent
Along with a discussion, examples of real-life tactical and operational decisions involved in the integrated approach to drug development will be presented.
What are some key supply considerations that sponsors need to keep in mind when planning a DCT? What should they look out for when choosing a supply partner?
This webinar on May 1 will explore several alternative clinical supply models, use cases and identify key considerations when adopting one of these models.
As the cell and gene therapy market continues to grow, analytical science will play an increasingly important role.
This ebook analyzes how to drive the industry toward optimizing delivery of injectable products and, ultimately, improving patient care.
The oral solid dose market is robust due to demand for specialized dosage forms such as controlled release, pediatric and geriatric delivery vehicles.
The constant drive for efficiency has become an essential element of any business process, across all industries.
Cell and gene therapies represent the next-generation of therapeutics.
The Importance of Risk Assessment and the Role of Evaluating Elemental Impurities
Analytical technology and processes are evolving as the biologics industry continues to grow.
As the biologics market grows, the demand increases for development and manufacturing capabilities.
Underscores the company’s commitment to delivering ‘unparalleled’ customer service.
By: Charlie Sternberg
Partnership expected to improve yield and upgrade analytical methods ahead of clinical use and regulatory submissions.
Purchases a GEA Pharma-SD type PSD-4 solvent-capable spray dryer designed to produce commercial batches up to 500 kg.
By: Kristin Brooks
Will house process development and analytical services for advanced peptide API production from development through commercialization.
Wang brings nearly 20 years of Wall Street sell-side experience.
By: Patrick Lavery
Adds raw material and finished product testing capabilities for pharmaceutical, biopharmaceutical, and related industries.
Joanne brings more than 25 years of pharmaceutical industry experience to the role.
Strengthens its global pharmaceutical platform and expands its presence in infectious diseases.
Combined platform connects patients, clinicians and biopharma partners—creating a real-world network for precision medicine execution and outcomes.
How Coperion’s single-source approach helps CDMOs and pharma manufacturers reduce complexity, accelerate scale-up, and support both batch and continuous operations.
Released By Coperion
VIR-5500 is an investigational PRO-XTEN dual-masked CD3 T-cell engager (TCE) targeting PSMA for the treatment of prostate cancer.
PAI took place over four days for an API that the Malvern, PA site will manufacture for a global pharma company.
Bora acquired a Mississauga, Ontario facility from GSK in 2020.
The Human Health organization will be split between Oncology and Specialty, Pharma & Infectious Diseases business units.
Summit Pharmaceuticals to distribute PL BioScience’s ELAREM Ultimate-FD PLUS and broader ELAREM portfolio for clinical applications.
Chief Operating Officer Yair Heller has been elevated to CEO, and co-founder Joseph Mossel will lead the biopharma division.
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