
GMP Audit Services.
ICE Pharma Group performs good manufacturing practice (GMP) audits at supplier sites in China and India to ensure GMP compliance. Our team of experts conducts Full Site audits focusing on a facility’s quality management systems (QMS).
Our commissioned audit service allows our clients to customize an exclusive audit that is tailored to their requirements. Our clients can request various audits including:
- API Manufacturing
- Excipients Manufacturing
- Sterile Product Manufacturing
- Non-sterile Product Manufacturing
- Primary Packaging Organisations
- Contract Manufacturing Organisations
Our Audit Process
The steps below highlight the IPG auditing process as well as client actions:
- Prior to conducting a commissioned audit, the client must fill in this Audit Quote form
- A detailed scope and standard for the audit are agreed between the client and IPG
- Client signs the relevant contract and confidentiality agreements
- The audit is carried out according to the agreed scope and timelines
- An interim report is produced by IPG
- The audit report and remedial action is finalised
- The audit report is sent to client
- Updates and audit closure statement is sent to client