Review on Good Documentation practice in pharmaceutical manufacturing unit as per European Union GMP Chapter-4 on Documentation

Documentation and Records: Harmonized GMP Requirements

'If it's not written down, then it didn't happen!' The basic rules in any good manufacturing practice (GMP) regulations specify that the pharmaceutical manufacturer must maintain proper documentation and records. Documentation helps to build up a detailed picture of what a manufacturing function has done in the past and what it is doing now and, thus, it provides a basis for planning what it is...

Literature Review on Patient-Friendly Documentation Systems

6 Survey of laymen/expert (e.g. patient/doctor) ontology translation systems 60 7 Empirical studies with patients on information provision 62 7.

Medication review and documentation in physician office practice.

CONTEXT Adverse drug reactions and drug-drug interactions are common. Medication-induced morbidity might be prevented through the documentation of medicines in the medical record and review of the medical record before new medications are prescribed. PRACTICE PATTERN EXAMINED Documentation and review by primary care physicians of patient use of prescription drugs, over-the-counter drugs (OTCs...

Cooperation as a Solution to the Problems of European Documentation

Showing Making: On Visual Documentation and Creative Practice

This article discusses visual representations of creative practice as source material to study the complex procedures involved in the making of artifacts. After a brief discussion of theoretical approaches to production processes, the genre of showing making is introduced as a new line of enquiry. The still and moving images belonging to the genre contain at least four main elements which are e...