Scientific Leadership

Guided by Senior Analytical Scientists & QA Authorities.

Our multidisciplinary leadership brings over two decades of pharmaceutical research, cGLP laboratory governance, and computerized data integrity oversight to every analytical test.

21 CFR Part 11 Lead Auditors
Shimadzu & Lab India Qualified
Ph.D. & M.Sc. Analytical Chemist Directorate
20+ Years Exp
RK
Managing Director

Dr. Rajesh Kumar

Visionary leader with 20+ years of expertise in pharmaceutical analytical chemistry, GLP operations, and global regulatory submissions.

Pharmaceutical Chemistry
cGLP Operations
Method Validation
Central Lab, Vapi
16+ Years Exp
PS
Head of QA & Compliance

Dr. Priya Sharma

Quality assurance specialist with deep expertise in 21 CFR Part 11 data integrity, ISO/IEC 17025 accreditation, and audit readiness.

21 CFR Part 11 Audit Trails
ISO/IEC 17025
Regulatory Clearances
Central Lab, Vapi
15+ Years Exp
AP
Head of Analytical Research

Dr. Amit Patel

Chromatography and spectroscopy authority with 15+ years in method validation, forced degradation, and trace elemental analysis.

HPLC / GC-HS Chromatography
ICP-OES Trace Elements
Stress Degradation
Central Lab, Vapi
Direct Scientific Consultation

Have a challenging chromatographic separation or regulatory query?

Speak directly with our technical heads to discuss custom method transfer, forced degradation, or elemental impurity protocols.

Consult Our Technical Head