1-ICH-International Council Of hormonisation 2. jaliya wala baag event - 13 April 1919 3. 21CFR Part 211 - cGMP of finished pharmaceuticals 4. ICH guideline - quality,equity,safety, management 5. Regulatory authority of Japan - PMDA (PHARMACEUTICALS AND MEDICAL DEVICE AGENCY) 6. HMPV Virus full form - HUMAN META PULMUNOVIRUS R han mam aapke jourics ke class jb se mai ataind ki hu mujhe jourics itni intrestingl lagne lagi hai ki aako kitna bhi thanks bolu Kam hi hai ...thankuso much mam ... 🙏🙏🙏🙏
1. ICH- international council for harmonisation of technical requirement of pharmaceutical for human use 2.jallianwala bagh massare: 13 April 1919 3.21CFR part 211-cGMP of finished pharmaceuticals 4. 4 guidelines under ICH: QSEM 5. Japan regulatory authority- MHLW 6. HMPV: human metopnemono virus.
1.International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. 2.13 April, 1919. 3.For CGMP-quality requirements for manufacturing pharmaceutical drugs. 4.4 Guidelines under ICH-Quality, Safety, Efficacy, Multi disciplinary. 5.Japan Regulatory Authority- Ministry of Health , Labour & Welfare. 6. HMPV Virus- Human Metapneumono Virus.
ICH= International Council of harmonisation of Technical Requirements For Pharmaceutical For Human Use Jaliwan bag =13 April 1919 21 CFR 211parts = Code For Federal Regulation 4 guidelines for ICH = Quality Safety Efficacy Multidispencr Japan = Ministry of Health & Family Welfare Hmpv= Human Meta pneumovirus
1-ICH-International Council Of hormonisation
2. jaliya wala baag event - 13 April 1919
3. 21CFR Part 211 - cGMP of finished pharmaceuticals
4. ICH guideline - quality,equity,safety, management
5. Regulatory authority of Japan - PMDA (PHARMACEUTICALS AND MEDICAL DEVICE AGENCY)
6. HMPV Virus full form - HUMAN META PULMUNOVIRUS
R han mam aapke jourics ke class jb se mai ataind ki hu mujhe jourics itni intrestingl
lagne lagi hai ki aako kitna bhi thanks bolu Kam hi hai ...thankuso much mam ...
🙏🙏🙏🙏
PMDA (Pharmaceuticals and Medical Devices Agency) is Japanese regulatory agency, working together with Ministry of Health, Labour and Welfare
Thank you ma'am
4, quality, safety,efficacy, multi disability
5, ministry of health and labour welfare
6, human metapneumenia 🦠 virus
1,ich- international council for harmonisation for technical for human use
2, 13 April 1919
3,cgmp of finished pharmaceuticals.
21 cfR - cgmp of finished pharmaceutical
177 is A R1 is only for medical devices
IcH - international council for harmonization for technical for human use
Jallianwala bagh- 13 April 1919
International Conference on harmonization
1. ICH- international council for harmonisation of technical requirement of pharmaceutical for human use
2.jallianwala bagh massare: 13 April 1919
3.21CFR part 211-cGMP of finished pharmaceuticals
4. 4 guidelines under ICH: QSEM
5. Japan regulatory authority- MHLW
6. HMPV: human metopnemono virus.
1.International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use.
2.13 April, 1919.
3.For CGMP-quality requirements for manufacturing pharmaceutical drugs.
4.4 Guidelines under ICH-Quality, Safety, Efficacy, Multi disciplinary.
5.Japan Regulatory Authority- Ministry of Health , Labour & Welfare.
6. HMPV Virus- Human Metapneumono Virus.
Q151 C
No audio for this lecture please checking solved gdc thank you so much ❤❤❤
152 D
W171 C
Q155 A
Management, quality safety efficacy , human Meta nimuno virus
Q159 b
Q166 1949
ICH= International Council of harmonisation of Technical Requirements For Pharmaceutical For Human Use
Jaliwan bag =13 April 1919
21 CFR 211parts = Code For Federal Regulation
4 guidelines for ICH = Quality Safety Efficacy Multidispencr
Japan = Ministry of Health & Family Welfare
Hmpv= Human Meta pneumovirus
Q 2010
159 b
can anyone write the all dates of editions of pharmacopeia
Q 177 answer?
Q158 D
Q154 D
169 b
Q161 D