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Stability storage disaster recovery to keep samples safe

Do you have a disaster recovery plan to cover a chamber breakdown or emergency failure in your stability storage process? What happens when unforeseen events interrupt your stability study? The..

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Storage of Reference and Retain Pharmaceutical Samples

Definitions Reference samples are retained to fulfil two purposes; firstly to provide a sample for analytical testing and secondly to provide a specimen of the fully finished product. They serve..

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Construction of Stability Storage Chamber

We have recently increased the capacity of our facility at Q1 Scientific, with the introduction of Stability Rooms #30 and #31. (more…)..

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Introducing an Alarmed Central Monitoring System

Q1 Scientific is a pioneer in the Irish industry and is a world leader in the provision of stability storage for the Pharmaceutical, Medical Device and Life Science industries. As..

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3 Award nominations for Q1 Scientific

Q1 Scientific Shortlisted for 3 National Awards (more…)..

GMP-compliant stability storage chamber used in pharmaceutical disaster planning for stability storage

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Increasing Stability Storage Capacity

Installing Stability Storage Chambers – Factors to Consider Q1 Scientific is a stability storage facility, providing industry-leading temperature-controlled storage. Over the years we have installed over 30 walk- in stability..

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Controlled Environmental Storage for Shelf-Life Studies for Food

Shelf-life is the period of time over which food maintains its safety and/or quality under reasonably foreseeable conditions of distribution, storage and use. The shelf-life begins from the time the..

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HPRA & FDA Mutual agreement between EU and US

Multual Recognition Agreement (MRA) HPRA / Ireland has been listed by the US Food and Drug Administration (FDA) as part of the mutual recognition agreement between the EU and the..

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HPRA Update on regulatory oversight of outsourced storage of stability samples

"A site that carries out storage of stability samples is not required to hold a GMP certificate for this activity in Ireland" (more…)..

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Stability testing requirements for Pharmaceuticals and Medical Devices

Development phase Accelerated stability tests provide a means of comparing alternative formula-dons, packaging materials, and/or manufacturing processes in short-term experiments. As soon as the final formulation and manufacturing process have..

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Forced degradation studies for Drug Substances and Drug Products

Forced Degradation Forced degradation is an important part of the drug development process as it provides knowledge about the degradation chemistry of drug substances and drug products. (more…)..

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ICH Requirements for Pharmaceutical

ICH refers to The International Council for Harmonisation, which regulates the Technical Requirements for Pharmaceuticals for Human Use. The ICH was founded in 1990 with the aim to internationally harmonise..

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About Q1 Scientific

Latest

Stability storage disaster recovery to keep samples safe

Storage of Reference and Retain Pharmaceutical Samples

Construction of Stability Storage Chamber

Introducing an Alarmed Central Monitoring System

3 Award nominations for Q1 Scientific

Increasing Stability Storage Capacity

Controlled Environmental Storage for Shelf-Life Studies for Food

HPRA & FDA Mutual agreement between EU and US

HPRA Update on regulatory oversight of outsourced storage of stability samples

Stability testing requirements for Pharmaceuticals and Medical Devices

Forced degradation studies for Drug Substances and Drug Products

ICH Requirements for Pharmaceutical

Q1 Scientific expands European operations with 4,000 sq m stability and GDP storage extension in Belgium

Choosing a Stability Storage CDMO: 5 Questions to Ask

Q1 Scientific celebrates double win at Pharma Industry Awards

Q1 Scientific Shortlisted for four Pharma Industry Awards