Tablets & Capsules Solid Dose Digest, Proof-of-Concept Services Q&A

Originally published on 12/10/2018 at Tablets & Capsules Solid Dose Digest, and appears in the December edition of Tablets & Capsules Solid Dose Digest newsletter

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Knowledge and Experience Equal Successful Technology Transfer

Originally published on 10/26/2018 at Pharma's Almanac

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Increasing Customer Successes Through Enhanced QC Agility and Flexibility

Originally published on 10/2/2018 at Pharma's Almanac

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Outsourcing Formulation Development & Manufacturing: CDMOs Are Innovating for 21st-Century Medicine

Originally published on 6/6/2018 at Drug Development & Delivery

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Scientific Expertise Facilitates Oral Peptide Product Development and Manufacturing

Originally published on 5/29/2018 at Pharma's Almanac

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Oral Solid Dosage Manufacturing

Originally published on 5/25/2018 at Pharmaceutical Outsourcing

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Five Minutes With Jim Gregory, CEO, UPM Pharmaceuticals – DCAT Week ‘18

UPM Pharmaceuticals CEO- Jim Gregory interviewed by Pharma Horizon Journal during DCAT week 2018.

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Facilitating Implementation and Customer Service with Offline Serialization

Originally published on 3/12/2018 at Pharma's Almanac

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UPM Pharmaceuticals appoints Daniel Dixon as Vice President of Quality Control

UPM Pharmaceuticals, a Contract Development and Manufacturing Organization (CDMO) focused on solid oral and semi-solid drug dosage forms, has appointed Daniel Dixon to the position of Vice President of Quality Control.  Mr. Dixon will oversee UPM's Analytical Testing & Development groups and the Microbiological & Raw Material Testing Labs.

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A CDMO’s Small-Town Environment With Big-Time Operations

Originally published on 11/03/2017 at Pharmaceutical Processing, and appears in the November/December issue of Pharmaceutical Proccessing

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