Durgadevi Ganesan

third party certification autonomous body international accreditation laboratories accredited laboratories iso 17034 iso/iec 17043 iso 15189 iso/ iec 17025 nabl accreditation process quality assurance benefits of nabl certification reference material producers proficiency testing providers medical testing laboratories calibration laboratories testing laboratories national accreditation board nabl quality risk joseph m juran design principle of qbd control strategy design space design tools design of experiments pat qrm cpp cqa qtpp objectives of qbd elements of qbd ich q10 ich q9 ich q8 qbd quality by design iso certified iso registration benefits of iso 9000 & 14000 elements of iso 9000 & 14000 iso 9000 series iso standards iso certification steps for registration of iso 14000 9000 qms ems environment quality management system registration of iso 14000 registration of iso 9000 international standards iso 14000 iso 9000 iso stability testing of new drug photostability testing stability for new dosage form climatic zones iii & iv evaluation of stability data bracketing matrixing q1f q1e q1d q1c q1b q1a stability guidelines ich stability testing guidelin ich guidelines ich stability testing stability testing stability ich retinoic acid phylloquinone menaquinone vitamin deficiency diseases recommended dietary allowance biochemical functions of vitam coenzyme form of vitamins chemical nature tocotrienols tocopherol ergocalciferol cholecalciferol retinal retinol fat soluble vitamin vitamins vitamin-k vitamin-e vitamin-d vitamin-a vitamin-b protocol for hr-ms based approach protocol for lc-ms analysis in-vivo metabolite identification enzyme-assisted extraction ultrasound-assisted extraction microwave-assisted extraction laser micro dissection dried blood spot in vivo sampling hybrid spe dispersive solid phase extraction protein precipitation liquid liquid extraction (lle) sample preparation methods sample preparation and protocols in metabolite ide clinical significance determination of bioequivalence of a drug product importance of bioequivalance studies need for bioequivalence studies reasons to perform bioequivalence studies bioequivalence clinical significance of bioequivalence studies difference between parallel and crossover study de replicate crossover study design balanced incomplete block design (bibd) two-period crossover study design latin square desin cross-over studies parallel design study design design of pharmacokinetic studies crossover study design reporting degradation products contents of batches analytical procedures threshold for degradation products in new drug pro identification of degradation products reporting procedure rationale for the reporting and control of degrada esi apci atmospheric pressure photo ionization appi maldi fab ei electrospray ionization atmospheric pressure chemical ionization matrix associated laser desorption ionization fast atom bombardment field ionization chemical ionization electron impact ionization mass ionizers ionization techniques categories of ion sources mass spectrometry invitro drug release testing rug release testing alternative methods of dissolution testing and tra non official methods official methods dissolution mass analyzers mass analysers 2d ion trap 3d ion trap ft-icr tof ion trap mass analyzer fourier transform ion cyclotron resonance orbitrap mass analyzer time of flight mass analyzer quadrupole mass analyzer mass analyzer applications of mtt assay advantages and limitations cytotoxicity assay significance trouble shooting interpreting values mtt assay procedure mtt assay protocol reagents and preparation principle of mtt assay cell viability assay mtt assay cyanocobalamine folic acid pantothenic acid biotin pyridoxine niacin riboflavin thiamine vitamin b12 vitamin b9 vitamin b5 vitamin b7 vitamin b6 vitamin b3 vitamin b2 vitamin b1 microbiological assay patentapplications typesofpatent patentee patent