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[ CourseWikia com ] Udemy - Technical Project Management For Generic Drug Development
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1 - Introduction
1 - 1-Introduct-on.pdf
1 - Introduction.mp4
10 - Analytical Studies for Generic Drug Development
58 - 10-1-PM-AnalyticalStudies.pdf
58 - Analytical Studies for Generic Drug Development.mp4
11 - Pilot Manufacturing for Generic Drug Development
59 - Pilot Manufacturing for Generic Drug Development.mp4
12 - Analysis of Pilot Batches for Generic Drug Development
60 - 12-1-PM-AnalysisofPilotBatches.pdf
60 - Analysis of Pilot Batches for Generic Drug Development.mp4
13 - Performing Bioequivalency Study for Generic Drug Development
61 - 13-1-PM-BioequivalencyStudy.pdf
61 - Performing Bioequivalency Study for Generic Drug Development.mp4
14 - Preparation Registration Dossier for Generic Drug Development
62 - 14-1-PM-RegistrationDossier.pdf
62 - Preparation Registration Dossier for Generic Drug Development.mp4
15 - Conclusion
63 - CONCLUSION-AYDANOZDEN.pdf
63 - Conclusion.mp4
2 - Introduction to Generic Drug Development
2 - 2-1-PM.pdf
2 - Active Pharmaceutical Ingredient API Finished Pharmaceutical Product FPP.mp4
3 - 2-2-PM.pdf
3 - Reference Listed Drug RLD Generic Multisource Pharmaceutical Products.mp4
4 - 2-3-PM.pdf
4 - Pharmaceutical Bioequivalency Therapeutic Equivalency.mp4
5 - 2-4-PM.pdf
5 - Reference Listed Drug RLD Development.mp4
6 - 2-5-PM.pdf
6 - Generic Drug Development.mp4
7 - 2-6-PM.pdf
7 - Comparision of Reference Listed Drug RLD Development Generic Drug Developmen.mp4
8 - 2-7-PM.pdf
8 - Invitro Invivo Studies for Drug Product.mp4
3 - Introduction to Project Management
10 - 3-2-PM.pdf
10 - Priorizitation of Project Pipeline.mp4
11 - 3-3-PM.pdf
11 - Project Phases.mp4
12 - 3-4-PM.pdf
12 - Project Manager.mp4
13 - Project Team Project Stakeholders.mp4
14 - 3-6-PM.pdf
14 - Project Management Tools.mp4
9 - 3-1-PM.pdf
9 - Project Elements of Project Cost Time Scope.mp4
4 - Project Management for Generic Drug Development
15 - 4-1-PM.xlsx
15 - Project Diary for Generic Drug Development.mp4
16 - 4-2-PM.xlsx
16 - Project Milestones for Generic Drug Development.mp4
17 - 4-3-PM.xlsx
17 - Project Gantt Chart for Generic Drug Development.mp4
18 - 4-4-PM.xlsx
18 - Generic Drug Development Project Phases.mp4
5 - Desk Research for Generic Drug Development
19 - 5-1-PM-DeskResearch.pdf
19 - Desk Research for Generic Drug Development.mp4
20 - 5-2-PM-DeskResearch.pdf
20 - European Medicines Agency EMA.mp4
21 - 5-3-1.pdf
21 - 5-3-2.pdf
21 - 5-3-PM-DeskResearch.pdf
21 - World Health Organization WHO Food and Drug Administration FDA.mp4
22 - 5-4-PM-DeskResearch.pdf
22 - Pharmacopoeias Dailymed.mp4
23 - 5-5-PM-DeskResearch.pdf
23 - Drugscom.mp4
24 - 5-6-PM-DeskResearch.pdf
24 - DrugBank.mp4
25 - 5-7-1.pdf
25 - 5-7-PM-DeskResearch.pdf
25 - Google Patents.mp4
26 - 5-8-PM-DeskResearch.pdf
26 - Espacenet.mp4
6 - Raw Material Selection for Generic Drug Development
27 - 6-1-PM-RawMaterialSelection.pdf
27 - Raw Material Selection for Generic Drug Development.mp4
28 - 6-2-PM-RawMaterialSelection.pdf
28 - Evaluation of Characteristics of API.mp4
29 - 6-3-PM-RawMaterialSelection.pdf
29 - Stability Characteristics of API.mp4
30 - 6-4-PM-RawMaterialSelection.pdf
30 - Evaluation of Suppliers of API.mp4
31 - 6-5-PM-RawMaterialSelection.pdf
31 - Evaluation of Inactive Ingredient and Packaging Material.mp4
7 - PreFormulation Studies for Generic Drug Development
32 - 7-1-PM-PreFormulationStudies.pdf
32 - PreFormulation Studies for Generic Drug Development.mp4
33 - 7-2-PM-PreFormulationStudies.pdf
33 - Characterization of RLD.mp4
34 - 7-3-PM-PreFormulationStudies.pdf
34 - Defining Quality Target Product Profile QTPP.mp4
35 - 74.mp4
35 - Evaluation of BE Requirements.mp4
36 - 7-5-PM-PreFormulationStudies.pdf
36 - Evaluation of Inactive Ingredient Required for Formula.mp4
37 - 7-6-PM-PreFormulationStudies.pdf
37 - Compatibility Study.mp4
38 - 7-7-PM-PreFormulationStudies.pdf
38 - Supplying New material Apparatus Equipment.mp4
39 - 7-8-PM-PreFormulationStudies.pdf
39 - Performing PreFormulation Trials.mp4
8 - Analytical Method Development Studies for Generic Drug Development
40 - 8-1-PM-AMD-Studies.pdf
40 - Analytical Method Development Studies for Generic Drug Development 1.mp4
41 - 8-2-PM-AMD-Studies.pdf
41 - Analytical Method Development Studies for Generic Drug Development 2.mp4
42 - 8-3-PM-AMD-Studies.pdf
42 - Literature Search for Analytical Method Development.mp4
43 - 8-4-PM-AMD-Studies.pdf
43 - Supplying Chemicals Materials Equipments.mp4
44 - 8-5-PM-AMD-Studies.pdf
44 - Performing Method Development Studies.mp4
45 - 8-6-PM-AMD-Studies.pdf
45 - Determining Acceptance Criteria.mp4
46 - 8-7-PM-AMD-Studies.pdf
46 - Determining Dissolution Parameters.mp4
47 - 8-8-PM-AMD-Studies.pdf
47 - Performing Stress Studies.mp4
48 - 8-9-PM-AMD-Studies.pdf
48 - Performing PreValidation Studies.mp4
9 - Formulation Studies for Generic Drug Development
49 - 9-1-PM-FormulationforGDD.pdf
49 - Formulation Studies for Generic Drug Development.mp4
50 - 9-2-PM-FormulationforGDD.pdf
50 - Performing Formulation Trials.mp4
51 - 9-3-PM-FormulationforGDD.pdf
51 - Optimizing Formulation by using QBD.mp4
52 - 9-4-PM-FormulationforGDD.pdf
52 - Supplying Chemicals RawMaterials Equipments for Pilot Manufacturing.mp4
53 - 9-5-PM-FormulationforGDD.pdf
53 - Preparing Formulations for Critical Material Attributes CMA.mp4
54 - 9-6-PM-FormulationforGDD.pdf
54 - Preparing Formulations for Critical Quality Attribute CQA.mp4
55 - 9-7-PM-FormulationforGDD.pdf
55 - Preparing Formulations for Critical Process Parameter CPP.mp4
56 - 9-8-PM-FormulationforGDD.pdf
56 - Discriminitive Dissolution Parameters.mp4
57 - 9-9-PM-FormulationforGDD.pdf
57 - Compatibility Study with Final Formula Components.mp4
Bonus Resources.txt
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