Examples of using Process validation in English and their translations into Indonesian
{-}
-
Colloquial
-
Ecclesiastic
-
Computer
-
Ecclesiastic
To general principles of process validation[6].
Of process validation considered acceptable by the FDA were outlined.
Guidelines on General Principles of Process Validation[1].
A copy of the process validation protocol, specific to this FPP, described below;
In front of the participant of SIKEP business process validation in Malang(5-6/07/2018).
The existence of process validation of concepts, laws, and principles that students constructed in cognitive structure.
Critical process parameters should be controlled and monitored during process validation studies.
With the emergence of the pharmaceutical process validation concept, the fol¬lowing four additional steps have been added.
The concept is alsorecognized in the FDA's Guidelines on General Principles of Process Validation[1].
The course will provide practical insights into how“modern process validation” is carried out and how to avoid common and costly mistakes.
(4) the important process parameters andprocess document feature values must pass a procedure qualification or process validation.
APICMO also provides process validation, quality studies, impurity studies and stability studies to meet customer IND and NDA requirements.
Qualification is often a part(the initial stage) of validation, butthe individual qualification steps alone do not constitute process validation.
The formalized process validation program should never be under taken unless and until the following operations and procedures have been completed satisfactorily.
This knowledge forms the basis of the manufacturing process, control strategy, process validation approach, and ongoing continual improvement.
Process validation should be conducted in accordance with Section 12 when batches are produced for commercial use, even when such batches are produced on a pilot or small scale.
In these cases,the organization must ensure the control over the outsourced process includes process validation in accordance with ISO 9001:2000 clause 7.5.2.
If the process validation studies have already been conducted(e.g. for sterile products), a copy of the process validation report should be provided in the PD in lieu of 1. and 2. above.
Qualification is often a part(the initial stage) of validation, butthe individual qualification steps alone do not constitute process validation(World Health Organization).
A repeat of the process validation to provide an assurance that changes in the process/ equipment introduced in accordance with change control procedures do not adversely affect process characteristics& product quality.
In these cases,the organization needs to ensure that the control over the outsourced process includes process validation in accordance with ISO 9001:2015 clause 8.4.2.
In prospective process validation, an experimental plan called the validation protocol is executed(following completion of the qualification trials) before the process is put into commercial use.
(f) Provide knowledge to enhance process understanding, enrich the design space(where established),and enable innovative approaches to process validation.
It is designed to provide an overview of the latest concepts andguidance documents for Process Validation as issued by the EU and PIC/S PE 009 Annex 15 in October 2015, as well as the US FDA in 2011.
According to the process validation results and customer feedback, on the basis of the first generation prototype developed the second generation of the new machine, every minute can produce more than 50 meters products, more than mainstream imported equipment.
A procedure should be established for retaining all appropriate documents(e.g., development history reports, scale-up reports,technical transfer reports, process validation reports, training records, production records, control records, and distribution records).
Sources of knowledge include, but are not limited to, prior knowledge[…], pharmaceutical development studies,technology transfer activities, process validation studies over the product lifecycle, manufacturing experience, continual improvement, and change management activities.
We own various kinds of inspection and testing facilities with value over USD10million, now, 16 testing tables, 6920 gear testing centre, X ray detecting machine, high speed dynamic balancing machine, ultrasonic flaw detection machines, etc, we are equipped with complete testing, inspection, analysis control system, advanced testing machines and simulative working condition test table and automatic control testing system,which guarantees our new product research, processing validation and quality.