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Quality planning best practice for medical device and GMP

GMPSOP

This article provides an in-depth look at how you, as a professional in a GMP business, can prepare quality planning documentation, especially from the perspective of a medical device manufacturing business. Additional documents included each month. Documentation control b. Additional documents included each month.

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How to conduct GMP training for employee

GMPSOP

Additional documents are included each month. Work, Health and Safety: The WH&S manager or specialist proposes and conducts a safety and environment training program that meets the WH&S and Environment compliance requirements as regulated by the local authorities. . All are written and updated by GMP experts.

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NHC Comments on the Federal Evidence Agenda on Disability Equity

Putting Patients First Blog

As an organization dedicated to advocating for patients and promoting patient-centered health policy, we fully support the Office of Science and Technology Policy (OSTP)’s initiative to gather insights and develop a comprehensive agenda that advances disability equity. 15 (Directive No.

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Digital Transformation in Clinical Trials: Advancing Healthcare with Technology

Viseven

In the pre-digital era, clinical trials relied on traditional methodologies centered around in-person interactions and manual data collection, which presented numerous limitations. Data collection involved paper forms, diaries, and in-person interviews , which, while essential for documenting symptoms and outcomes, were prone to human error.