Our Services

QuicQ GMP Consultancy directors have vast experience of developing quality management systems for regulatory compliance in the pharmaceutical industry. It can help you in different ways to improve the compliance and efficiency of your processes:

• Plan and establish an effective quality management systems
• Review of existing quality management systems in view of compliance and efficiency
• Perform root cause analysis to investigate a process/laboratory failure and help to identify the right actions
• Conducting on-site Audit for Gap Assessment and Pre-inspection Audits for inspection readiness
• Conducting GMP Audits/Vendor Audit
• Suggest solutions to meet the regulatory requirements and Strengthening the quality systems
• Writing of response for regulatory inspection audits and customer audits
• Process / System Optimization and Improvement for GXP regulatory compliance
• Building the capabilities of the employees through training on cGMP and various regulatory topics

QuicQ Consultants can conduct a variety of audits on your behalf in any country. We execute the audit plan agreed with the client to its finesse keeping in mind your relationship with the vendors. With the vast experience of conducting for-cause audits and investigations, you can rely on us to take complex compliance issues to conclusion.

• Conducting GMP Audits/Vendor Audit
• Suggest solutions to meet the regulatory requirements
• Writing of response for regulatory inspection audits and customer audits
• Data Integrity Audit in various functions
• Can work as a quality and regulatory representative in your due-diligence team while in-licensing or out-licensing a product

• Establishment of the Laboratory Control systems
• Establishment of the Microbiology Laboratory
• Establishment of the Stability Functions
• Productivity Enhancement Services through adopting principles of Six Sigma
• Review of Laboratory data includes Electronic data with respect to data Integrity Prospects and Regulatory Expectations.

• Support in Plant Qualification Process
• Support in Equipment Qualification Process
• Support in Laboratory Qualification Process
• People and Process Qualification documentation