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Pace® Life Sciences Announces Compliant US FDA Inspection of Operations in Oakdale, MN

Proven track record of consistent high quality confirmed at Pace® Life Sciences headquarters MINNEAPOLIS, MN., July 25, 2024 (NEWSWIRE.COM): Pace® Life Sciences, a full-service FDA-registered GMP Analytical Testing laboratory and contract development and manufacturing organization (CDMO) and a Division of Pace®, a Science and Technology Company, announced today a successful inspection from The Food &

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Dean Bornilla, Pace Life Sciences.

Pace® Life Sciences Division Names Dean Bornilla as Head of Commercial

Bornilla brings over 25 years of commercial pharmaceutical experience to Pace® MINNEAPOLIS (July 23, 2024) – Pace® Life Sciences, a full-service contract development and manufacturing organization (CDMO) and a Division of Pace®, a Science and Technology Company, announced today that Dean Bornilla has been named Head of Commercial reporting to Dawn Von Rohr, President, Pace® Life

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Viscosity

Viscosity Testing to Achieve Ideal Performance Predict your product’s sensitivity to temperature fluctuations, moisture control, dissolution of material, and homogeneity of solution with help from our expert team. We perform viscosity testing with a variety of different methodologies and are compliant with compendial methods, including: USP Viscosity – Capillary Methods USP Viscosity – Rotational Methods

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Photostability Testing

Photostability Analysis by ICH Q1B Standards Satisfy ICH Q1B standards with expert photostability testing for your drug product. Photostability studies are performed as part of forced degradation studies, product development, or product investigation and complaint handling. We employ photostability chambers that are temperature-controlled with calibrated UV and visible light sources. These studies are executed based

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