1. Method development & validation (MD/MV) ICH Q2R (1), USP <1225>, ORA guidelines.
2. Method verification and Method transfer USP <1224>, USP <1226>.
3. Nitrosamines with Gas Chromatograph Mass Spectrometer.
4. Packaging Material Testing IP, BP & USP < 661.1>, <661.2>.
5. 5 Batch analysis and Batch Release.
6. API’s and Excipients testing as per USP, BP and IP.
7. Residual Solvent analysis as per USP <467>.
8. Metal Impurities USP <233>.
9. Formulation Product development studies.
10. Stability testing as per ICH Q1.
11. Dissolution studies.
12. Forced degradation studies.
13. Testing of materials as per Pharmacopeia.
14. Cleaning or residue Method Development and Validations.
15. Complete Water Analysis.