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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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Staying abreast of regulations with NGS?based viral safety for faster, safer and more ethical lot release of our vaccines

European Pharmaceutical Review

A typical example is the classical biosafety animal testing driven by a collection of guidance documents that often were not revised for decades (eg, ICHQ 5A). However, the biosafety testing strategies rely on outdated technologies that have remained unchanged for decades. In vivo and in vitro tests were very powerful when first implemented.

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How Can I Earn CME Credits?

Board Vitals - Pharmacist

Events sponsored by an accredited CME provider include national, regional, or local conferences, workshops, seminars, journal clubs, simulation labs, and live webinars. This method is truly a type of self-directed learning in which you document a clinical question, the sources consulted, and the application to your practice. .

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Time to change the channel? The future for customer engagement models

pharmaphorum

Documenting the change in pharma’s engagement of HCPs is one thing – predicting where channel mix goes in the future, the most important question, is quite another. Preference shifts for the other two groupings, meetings events and seminars (in person or remote) and published medical content, see some, but much more minor, shifts.