Development of Pharmaceutical products

  1. Contract development including lab and pilot scale experiments according to the International Conference on Harmonization (ICH);
  2. Scale up and technology transfer;
  3. Innovative formulation /process development;
  4. Product troubleshooting;
  5. Process optimization.
  1. Method development and validation (HPLC, GC, Spectrophotometric, Titration);
  2. Comparative dissolution and bio-waiver experiments and reports;
  3. GC Residual solvents.

Conducting stability testing of pharmaceutical products and storage condition stability, according to the International Conference on Harmonization (ICH) at different storage conditions (30C° / 65% RH, 30C° / 75% RH, 40C° / 75% RH).

  1. Preparation and / or reviewing of CTD files;
  2. File registration at MOHE and following up.

SDIPI invest in a complete set up for conducting comparative dissolution profile for semisolid preparations using Franz diffusion cell according the MOHE requirements.