All pocket books are sized at 4′ X 6′ with coloured water proof cover with readable font size.
WHO GMP requirements – contains main GMP principles as mentioned in TRS 961, HVAC requirements for non-sterile products and good storage practices as mentioned in TRS 908 Annex 9
ICH quality guidelines – contains Q8- Pharmaceutical Development, Q9-Quality Risk Management and Q10-Pharmaceutical Quality Systems
Indian GMP requirements – Schedule M – GMP requirements of premises, plant and equipment for pharmaceutical products, M1-Homeopathic preparations, M2 – Cosmetics, M3 – Medical devices, N- Pharmacy and Schedule L1 – GLP
US FDA GMP Regulations and Guidelines – 21 CFR Part 210 & 211, Sterile medicinal products manufactured by aseptic processing and Process validation requirements R1.
GMP for API – ICH Q7 plus ICH Q11 – ( Development and manufacturing of API ).