Documentation Of Various Pharmaceutical Dosage Forms According To Ich Guidelines
This study describes the documentation required for various dosage forms according to ICH Guidelines. The main aim of the documentation to increase the productivity and profits of pharmaceutical products and minimize the loss of investments. The document is help in planning, controlling, and co-coordinating of the material and production management in any firm. They are also help to increase the planning. The various dosage form included are tablet, capsule, creams, ointments and ophthalmic preparations. The various documentation involved according to ICH guidelines are Quality control test, BFR, MFR etc... By viewing this study, the documentation procedure is clear, ambiguous according to ICH guidelines.
2022-12-31 — Updated on 2022-12-31
How to Cite
Anuvab Dey , Dharani S , M.J. Aaliya Parvin , Shilpi Rituparna Roy , Vaibhav Kumar Satyanshu , Akshaya Devi R , Sonia K. (2022). Documentation Of Various Pharmaceutical Dosage Forms According To Ich Guidelines. Journal of Pharmaceutical Negative Results, 4664–4674. https://doi.org/10.47750/pnr.2022.13.S10.565