What is Process Verification

According to FDA process verification is defined as confirmation by examination and provision of objective evidence that specified requirements have been fulfilled
process verification

Benefits of CSV in the Pharma industry

  • Making sure that actual results meet the specifications or not and if not finding the deviation between actual results and specifications

Services

We are Specialised in delivering the following Automation Services

1

Control Module Software Design Specification , Configuration and Testing

2

Common Composite (EM/CM) Design Specification

3

Phase Class Software Design Specification , Configuration and Testing

4

Equipment Module Class Software Design Specification , Configuration and Testing

5

Phase Software Design Specification and Coding

6

Graphic Design Specification and Configuration

7

CMI Software Design Specification and Configuration

8

Internal Testing of EM and Phases

9

Unit Module Software Design Specification and Coding

10

Recipe Testing

11

Control Module Configuration

12

Interlock Configuration and Testing

13

IQ and OQ for Solvent Transfer Sequence

14

DSATP Protocol Creation

GET IN TOUCH

ABOUT US

Based in Ireland We are Leading in Automation Services for Pharmaceutical Companies in Computer System Validation , Installation Qualification , Operational Qualification and Process Verification

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