Customisable and tailored consultancy
Thanks to our considerable worldwide experience, DOC can offer a wide range of consultancy services. These are specifically tqargeted towards troubleshooting, gap analysis and recovery for existing facilities and processes. Our aim is to help clients maintain compliance as regulatory requirements are modified, or to compensate for weak current situations.
Consultancy Services
With more than 25 years' experience gained from collaboration with leading firms, and relevant regulatory agencies and organisations, DOC can offer a proven range of consultancy services. Our qualified teams can mitigate risk, and respond to crisis or the regulatory changes that might have an impact on your business, for example, approval delays, recalls and deficiencies.
DOC can offer the following consultancy services:
- Pharmaceutical manufacturing system design review.
- Quality risk analysis.
- GMP process & system review.
- Existing facility audit.
- Validation master plan.
- Standard Operating Procedures (SOPs)/documentation preparation and support.
- Documentation of gap analysis & gap recovery plan elaboration.
- Data Integrity Compliance assessment.
- cGMP inspections preparation and corrective actions support.
For more information, please contact:
Christian Larsen - Email