Inspections are challenging processes that need to be taken seriously by the Pharmaceutical, Biotechnology, Medical Device Industries.
Nonconformities obtained by the organizations as a result of the audit may result in irrecoverable situations. Top Management who are aware of the results of the nonconformity caused by the audit results want to know in advance where the possible problems are. For this reason, it chooses to perform a detailed Mock Regulatory Inspection by an Independent and Specialized Company. As a result, the top management of the company takes precautions by anticipating the weak points and gaps in the processes.
Our Mock Regulatory Inspection and Gap Analysis service is finalized with a detailed report at the end of 5 days.
Overall Evaluation and Conclusion
With the application of Mock Regulatory Inspection & Gap Analysis, top management can obtain all the weaknesses of the facility very fast.
It sees the problems in advance that are likely to be encountered in the actual audits of the institutions such as FDA, MHRA, PIC / S, TMMDA etc. and ensures that action is taken for their solution.