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Patheon Overview Brochure

Liquid Large Volume Parenteral (LVP)

When your project is a Liquid Large Volume Parenteral, rely on Patheon for expertise in the development, optimization, and scale-up these complex formulations. Our broad experience spans a large number of projects and a variety of large and small molecules. In addition to our deep knowledge, we also offer the expansive resources, technologies, and range of forms and sizes to deliver exactly the right solution for your project. In fact, we often utilize this dose form to help our customers efficiently achieve proof of concept.

With a full range of equipment in the same facility, Patheon offers seamless scale-up from development to commercial manufacturing. This allows us to maintaining precision and accuracy of process conditions, while saving our customers time and money.

Capabilities

  • Analytical development
  • Formulation development
  • Biopharmaceutical development
  • Process design and clinical manufacturing
  • Commercial manufacturing
  • High potency compounds (category 3B)

Advantages

  • Wide range of vial sizes, including ISO standard vials
  • Full regulatory approval, including AIFA, ANVISA, Brazilian Sanitary Surveillance Agency, BSI, BSI/MDA, Canadian Ministry of Health, FDA, GCC States Health Authority, Health Canada (HPFBI), KFDA, MCA, MHRA, Saudi MOH, Taiwan Health Authority, TNO
  • Clinical and commercial batches filled on the same filling line
  • Option to commit to commercial batches while still in development
  • Simplified regulatory process

Ask The Experts

Anil Kane, Ph.D., MBA

Anil Kane, Ph.D., MBA
Dr. Kane has more than 25 years of experience in the science and business of taking molecules throug
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Kaspar van den Dries, Ph.D.

Kaspar van den Dries, Ph.D.
Based at our Tilburg facility in the Netherlands, Dr. van den Dries leads Patheon’s European researc
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Jason Vaughn, Ph.D.

Jason Vaughn, Ph.D.
Dr. Vaughn has expertise in early and preclinical development of liquid, semi-solid and solid dosage
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Roman Hlodan, Ph.D.

Roman Hlodan, Ph.D.
Dr. Hlodan is an expert in the development of biopharmaceuticals, including analytical method devel
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Stephen Closs

Stephen Closs
Mr. Closs possess more than 23 years of experience in formulation development, tech transfer, scale-
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William E. Weiser, Ph.D.

William E. Weiser, Ph.D.
Dr. Weiser is an expert in analytical method development and validation for APIs and drug products.
Read More »

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