Pharmaceutical Qualification Computerized Systems Validation (CSV) Integrated Quality System and its Implementation Plant Upgradation Third Party (3P) Auditing Inspection Readiness FDA 483 and warning letters Remediation Services Data Integrity Auditing Program GMP Training Programme

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PharmQS consulting team has rich experience in the highly regulated and reputed pharmaceutical companies in senior positions. Our experience helps you to cast an unbiased look into your processes and systems for successful and sustainable quality systems. We offer a customised comprehensive consulting services on challenges related to GxPs and regulatory compliance.

Our primary approach starts with Gap assessment or Mock Inspection to identify the gaps and areas where the current compliance status needs to be improved. The Assessment Report will summarize the gaps between existing system and the regulatory requirements and it also contains recommendations to close the gaps to meet various regulatory requirements like WHO-GMP/USFDA / MHRA / TGA /EMA / ANVISA etc.