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Life sciences is a vast and interdisciplinary field that encompasses a range of scientific disciplines that focus on the study of living organisms and their interactions with each other and their environment. Some of the key areas of study within life sciences include biology, biochemistry, genetics, and molecular biology. One of the main goals of […]
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An FDA audit is inevitable for any organization that manufactures or processes medical equipment, devices or drugs. Once the inspector enters the building, it might leave your leadership and team members feeling one of two ways: A calm excitement for the prepared organizations that are prepared and ready to successfully go through the audit, or […]
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The medical device industry landscape of regulations is constantly changing. The European Union’s Medical Device Regulations (EU MDR) came into effect on 26 May 2021 after a three-year transition period, is no exception. The EU MDR (formally, EU MDR 2017/745) replaced the EU’s Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices […]
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GMP audit
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5 benefits to implementing a GxP quality management system (QSM) software:
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Success or Death by CAPA
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Life Sciences Cyber resilience
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Precision Talent Group First Annual Harvestfest
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The life sciences industry is amazingly diverse and the demand for skilled Medical Writers is high. Medical writers work closely with scientists, doctors, and other groups in the medical and biotechnology profession, by curating a vast array of content that can cover patient information sheets, medical reports, clinical study reports, and regulatory submissions.
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It is not uncommon that in times of uncertainty, hiring managers trade off the cost of high-impact contingent staffing without consideration of the benefits of such a model. Alternatively, committing to a long-term contingent hire…
