ISO and FDA Current Good Manufacturing Practices (CGMP) presume that both the process and documentation that directs company processes follows pre-approved methods, and that any change to these methods is restricted to authorized personnel and tracked …
It focuses on document control processes within the quality system lifecycle and provides insight into the capabilities needed to automate change control processes that will increase efficiency, ensure compliance with regulatory requirements and improv…
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Many organizations seemingly face a devils’ bargain of needing to choose between producing applications that are secure and compliant or are completed on time. For embedded development teams to achieve quality and productivity goals simultaneously, they must both implement best practices and use proper tooling resources.
This report from VDC Research analyzes data from the recent Software and System Development Survey focusing on:
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Explore how the use of technology in the past decade or so has helped both regulated companies and regulatory agencies in easing the pains of delivering those products to patients and consumers worldwide. Regulatory milestones enforced by the FDA helped define the book’s scope. |
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This e-Book will explore how the use of technology in the past decade or so has helped both regulated companies and regulatory agencies in easing the pains of delivering those products to patients and consumers worldwide. Regulatory milestones enforced by the FDA helped define the book’s scope. |
This white paper shows how an optimized quality management system (QMS) can help a company avoid quality roadblocks and form the foundation for long-term regulatory compliance and, ultimately, for ensuring market success.Request Free!
This white paper proposes that an optimal quality management system (QMS) is the foundation for long-term regulatory compliance, and ultimately, for ensuring market success. Without a solid quality infrastructure, organizations are simply not equipped …
ISO and FDA Current Good Manufacturing Practices (CGMP) presume that both the process and documentation that directs company processes follows pre-approved methods, and that any change to these methods is restricted to authorized personnel and tracked …
It focuses on document control processes within the quality system lifecycle and provides insight into the capabilities needed to automate change control processes that will increase efficiency, ensure compliance with regulatory requirements and improv…
|
Many organizations seemingly face a devils’ bargain of needing to choose between producing applications that are secure and compliant or are completed on time. For embedded development teams to achieve quality and productivity goals simultaneously, they must both implement best practices and use proper tooling resources.
This report from VDC Research analyzes data from the recent Software and System Development Survey focusing on:
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