GxP-Blog

Blog
At record speed to the patient – development of a Transport Verification Master Plan (TVMP).
For the global introduction of a new pharmaceutical product, Chemgineering took on the important role of developing a master plan for transport verification.
Blog
Self-inspection of quality assurance in the pharmaceutical quality system
Periodic self-inspections of the pharmaceutical quality system are mandatory for pharmaceutical manufacturers in the EU
Blog
Quality Oversight in the GMP Quality System
This article describes , the measures that pharmaceutical manufacturers should implement in preparation for this requirement.
Blog
Deviations as essential quality parameters in the pharmaceutical quality system
This is the best way to prepare for the critical exam.
[Translate to Englisch:]
Blog
Data evaluation during GMP validation
In this way, unnecessary complications can be avoided as early as the selection of acceptance criteria.
Blog
Requirements for Hand Sanitizers – Often Underestimated!
Clarify requirements for hand sanitizers at an early stage
[Translate to Englisch:]
Blog
Careful management of specifications makes pharmaceutical products safe - Part 4
The "Careful handling of specifications in pharmaceutical quality systems“ theme is dealt with as a four part BLOG article. Read the fourth and final part of the blog series here.
[Translate to Englisch:]
Blog
Explosion protection – ATEX, EX zones, et al.
Duties of the plant operator with regard to explosion protection requirements.
[Translate to Englisch:]
Blog
Careful management of specifications makes pharmaceutical products safe - Part 3
The "Careful handling of specifications in pharmaceutical quality systems“ theme is dealt with as a four part BLOG article. Read the third part here.

This website uses cookies to provide you with the best possible experience. If you continue to browse our site, you consent to our use of cookies and to our privacy policy.