Precision analytical support
Independant consulting for method validation, transfer, stability studies and GMP documentation
QC & QA
pharmaceutical
for
GMP / GLP ANALYTICAL CONSULTING
Fast turnaround, inspection-ready documentation
Experienced support in quality & development
Expert support across the analytical lifecycle
Method development & validation
• Protocol and validation strategy support
• System suitability, robustness, and reporting
• OOS/OOT and root-cause documentation
• Transfer plans and acceptance criteria
Method transfer & troubleshooting
Stability study support
• Stability protocols and trend review
• Impurity monitoring and investigations
QC/QA & GMP Documentation
• Documentation review
• Clear data, compliant decisions
Research and development
• Innovative analytical solution & study design
• Identification of unknown impurities
From early development through regulatory submission — independent, GMP-compliant, and fast-turnaround
About Dr. Debbab
Ph.D. Analytical Chemistry, HHU-University, Duesseldorf, Germany
Former Researcher at Heinrich Heine University
Founded DEBBAB Consulting in 2015 to support pharma QC/QA & analytical development
More than 100 scientific publications & 5 international patents
