Udemy - Certificate Course in Veterinary Pharmacovigilance

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Free Download Udemy - Certificate Course in Veterinary Pharmacovigilance
Published 5/2025
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Language: English | Duration: 2h 58m | Size: 1.12 GB
Veterinary Pharmacovigilance, Animal drug safety, Veterinary drug surveillance, Veterinary medicine safety, VICH

What you'll learn
Introduction and Basics
Roles and Responsibilities, Scope, National legislation & Additional guidance
Setting-up a Pharmacovigilance system
Promoting Pharmacovigilance and Encourage reporting
Submission, Reception and Processing of Spontaneous reports
Recording PV data, Storage and Archival
Standardised Periodic Summary Reports (PSU)
Analysis of Aggregate data
Risk management and Follow-up regulatory measures
Communicating PV outcomes, Audits and Inspections
Requirements
Laptop/ PC/ Cellphone
Good Internet connection
Basic English
Description
Certificate Course in Veterinary Pharmacovigilance________________________________________________________________________________________________With growing global attention on animal health, food safety, and zoonotic diseases, the role of Veterinary Pharmacovigilance has never been more critical. This comprehensive course on "Veterinary Pharmacovigilance" equips you with the knowledge and skills needed to evaluate and report adverse drug reactions (ADRs) in animals, ensuring the safety of veterinary medicinal products.You'll explore the entire lifecycle of veterinary pharmacovigilance from identifying side effects in animals to complying with regulatory guidelines such as those from the EMA, FDA, and WHO. This course is ideal for veterinary professionals, regulatory affairs specialists, pharmacovigilance officers, and anyone involved in the development, use, or regulation of veterinary medicines.What You'll Learn:Introduction to Veterinary pharmacovigilance and its SignificanceRoles and Responsibilities, Scope, National legislation & Additional guidanceSetting-up a Pharmacovigilance systemPromoting Pharmacovigilance and Encourage reportingSubmission, Reception and Processing of Spontaneous reportsRecording PV data, Storage and ArchivalStandardised Periodic Summary Reports (PSU)Analysis of Aggregate dataRisk management and Follow-up regulatory measuresCommunicating PV outcomes, Audits and InspectionsWho Should Enroll?Veterinarians and animal health professionalsPharmacovigilance and regulatory affairs professionalsProfessionals from the veterinary pharmaceutical industryVeterinary students and researchersQuality assurance and compliance teams in animal healthcareWhy Take This Course?Learn from Real-world case examples and Expert guidanceGet certified in a highly specialized and growing domainEnhance your knowledge of Veterinary drug safety and regulationsContribute to safer Animal healthcare and Public health outcomesAdvance your career in Veterinary medicine or Pharmacovigilance with this niche and in-demand skill set.Enroll now and become a Certified expert in Veterinary Pharmacovigilance!
Who this course is for
Veterinarians and Animal health professionals
Pharmacovigilance and Regulatory Affairs professionals
Professionals from the Veterinary pharmaceutical industry
Veterinary Students and Researchers
Quality Assurance and Compliance teams in Animal healthcare
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5.13 GB | 37min 56s | mp4 | 1280X720 | 16:9
Genre:eLearning |Language:English​

Files Included :

Spoiler

1 About Drug Discovery Part 1.mp4 (42.66 MB)
2 History of Drug Discovery Part 2.mp4 (101.89 MB)
3 CRO and Sponsor Responsibilities Part 3.mp4 (58.24 MB)
4 Monitor Responsibilities Part 4.mp4 (155.27 MB)
5 History of Clinical Research Part 5.mp4 (272.64 MB)
54 WHO and ICSR Key Points on Signal Detection Part 1.mp4 (85.21 MB)
55 Risk Managemeny Part 2.mp4 (31.99 MB)
56 Coding in Pharmacovigilance Part 3.mp4 (37.3 MB)
57 Drug Dictionary Part 4.mp4 (193.11 MB)
58 Coding Using MedDRA Part 5.mp4 (65.14 MB)
59 General Considerations Part 1.mp4 (53.93 MB)
60 Safety Database Part 2.mp4 (163.48 MB)
61 ARISg & ARGUS Part 3.mp4 (41.18 MB)
62 Data Assessment Duplicate Check Part 4.mp4 (153.61 MB)
63 Assessment of Class Once Saved in ARISg Part 5.mp4 (44.44 MB)
64 Mandatory Field For Newcase Creation Part 6.mp4 (137.35 MB)
65 Duplicate Check Part 1.mp4 (24.98 MB)
66 Cases Part 2.mp4 (134.1 MB)
67 Product Table Part 3.mp4 (127.54 MB)
68 Product Table Part 1.mp4 (85.41 MB)
69 Worklist Part 2.mp4 (182.25 MB)
10 Lifecycle of Drug and Pharmacovigilance Part 5.mp4 (26.22 MB)
11 Need of Pharmacovigilance Even After Clinical Trials Part 6.mp4 (50.13 MB)
12 Do Pharmacovigilance Needed in Every Country Part 7.mp4 (20.33 MB)
13 Term & Definitions Part 8.mp4 (120.3 MB)
14 Term & Definitions Part 9.mp4 (36.39 MB)
15 Partners in Pharmacovigilance Part 10.mp4 (30.25 MB)
16 Drug Regulatory Authorities Part 11.mp4 (6.13 MB)
17 Pharmacovigilance Help & Rational Part 12.mp4 (43.1 MB)
18 What to Report Part 13.mp4 (14.74 MB)
19 History of Pharmacovigilance Evolution Part 14.mp4 (92.84 MB)
6 Problems Due to Inadequate PV System Part 1.mp4 (56.89 MB)
7 Active Ingredients Withdrawn Part 2.mp4 (21.76 MB)
8 Pharmacovigilance Definition Part 3.mp4 (46.64 MB)
9 Pharmacovigilance Aim & Responsbilites Part 4.mp4 (28.59 MB)
20 Principle Part 1.mp4 (199.08 MB)
21 Principle Part 2.mp4 (46.46 MB)
22 Sources of AE Reports Part 3.mp4 (23.46 MB)
23 Sources of AE Reports Part 4.mp4 (52.6 MB)
24 Timeline for ADR Reporting Part 1.mp4 (61.24 MB)
25 ICSR Report Part 2.mp4 (56.85 MB)
26 Form FDA Part 3.mp4 (27.53 MB)
27 ICSR Case Processing Workflow Part 4.mp4 (15.88 MB)
28 Receive Case Report Sources Part 5.mp4 (16.4 MB)
29 Safety Data Processing Part 6.mp4 (29.53 MB)
30 Receive Case Report Sources Part 7.mp4 (45.62 MB)
31 Sources of ICRSs Part 1.mp4 (46.69 MB)
32 Validity Criteria Part 2.mp4 (66.67 MB)
33 Steps in Triage Activity Part 3.mp4 (6.52 MB)
34 Steps in Triage Activity Part 4.mp4 (138.18 MB)
35 Regulatory Timelines Part 5.mp4 (26.78 MB)
36 Aggregate Reporting Part 6.mp4 (173.33 MB)
37 Narrative Writing Part 1.mp4 (76.82 MB)
38 Structure of A Narrative Part 2.mp4 (140.63 MB)
39 Example Part 3.mp4 (87.86 MB)
40 Introductory Paragraph Part 4.mp4 (29.01 MB)
41 Follow Up Narrative Part 5.mp4 (29.03 MB)
42 Follow Up Narrative Part 6.mp4 (4.68 MB)
43 Narrative Writing Part 7.mp4 (38.98 MB)
44 Why Need Regulation Part 8.mp4 (105.21 MB)
45 Labelling of Drugs Part 1.mp4 (74.08 MB)
46 Highlights for a Fictitious of Drug Part 2.mp4 (49.83 MB)
47 Example Part 3.mp4 (94.46 MB)
48 medDRA Process Flow Part 4.mp4 (49.87 MB)
49 Re-Assessment of Follow Up Part 1.mp4 (73.17 MB)
50 Example Part 2.mp4 (170.95 MB)
51 Signal Management Part 1.mp4 (96.36 MB)
52 Signal Management Part 2.mp4 (184.37 MB)
53 Risk Management Part 3.mp4 (124.58 MB)

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