Featured Articles
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The 3 Stages Of MES Analytics For Drug Manufacturing
6/14/2023
In order to access all of your organizations manufacturing data and insights, the most practical solution is a cost effective, modern MES for all lines and stages.
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Precision Medicine: Going Digital To Drive Innovation
6/2/2023
The Precision Medicine Initiative is driving forward the potential for a more customized health care approach, transforming the way health care professionals are treating diseases.
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Overcome 3 Key Challenges Facing Life Science Contract Manufacturers
6/2/2023
It has become clear that digitizing production processes is no longer optional for CMOs and CDMOs, but a necessity to keep up with the demand and competition in the pharmaceutical, biotechnology, and medical technology industries.
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Solving Biopharmaceutical Manufacturing Production Records Challenges
5/30/2023
Solve your companies manual manufacturing production records problems with modern manufacturing execution systems and gain the competitive advantage.
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Extending Quality Management Through Vendor Compliance Audits
5/25/2023
Explore the primary responsibilities of both manufacturers and vendors during a vendor compliance audit, as well as practical strategies and tools, including audit management software, that make them possible.
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Embracing And Implementing Computer Software Assurance Guidance
5/18/2023
Pharmaceutical manufacturers are exploring comprehensive computer software assurance (CSA) approaches, the benefits of implementing a risk-based framework, when to apply it, and the first steps to this CSA approach.
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Assess Your Digital Pharmaceutical Manufacturing Maturity
5/18/2023
Learn how regulated product manufacturers are meeting the demand for faster development and delivery of products to patients and where your operations fit in the digital maturity manufacturing model.
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5 Steps To Pass Your ISO 9001 Audit
5/18/2023
Reduce your pre-audit stress and pave the way to successfully meeting ISO 9001 standards and becoming certified.
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Transitioning To Pharmaceutical Validation 4.0
5/16/2023
To help companies achieve Pharma 4.0, the International Society for Pharmaceutical Engineering is driving Validation 4.0 as a way to help organizations expedite the computer software validation process.
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3 Paths to Patient Centricity in Pharma
4/10/2023
Learn about the benefits of patient centricity and an enterprise-wide approach to products, processes, and partnership that focuses on the patient perspective.