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MAIN ELEMENTS OF AN AIDIFY COURSE
Our courses support employees in learning more effectively by providing a range of tools and resources to help them succeed
Video
Our courses consist of bite-sized videos focusing on specific topics, providing short and engaging content that learners can easily consume and retain. With AIDIFY, you have the flexibility to learn at your own pace. Rewind and replay as needed for a complete understanding. The majority of them are in English.
Additional Learning Materials (ALMs)
AIDIFY's self-study resources offer access to a wealth of extra materials, expanding your knowledge on each topic. This includes up-to-date information on relevant legislation and articles, ensuring you have the latest and most accurate data to supplement your learning.
Presentation
Alongside our videos, AIDIFY's courses include professional presentations. They combine expert content with visual elegance, enriching your learning. This blend of audiovisual elements ensures a comprehensive learning experience, aiding in the effective absorption of the material.
Test
Each AIDIFY course concludes with a comprehensive test, assessing your grasp of the material and ensuring you've achieved the set learning outcomes. This evaluation not only solidifies your understanding but also boosts your confidence in applying the knowledge professionally.
Course Practice Activities (CPAs)
AIDIFY's CPAs are designed for practical application.
They deepen your engagement with course material and hone skills for real-world scenarios. By focusing on hands-on training, you gain valuable experience, equipping you to succeed in real-world applications and enhancing your professional expertise.
Certificate
Upon completing all units and passing the course test, you'll receive a certificate. It validates your mastery of the material, acting as a credential to showcase your skills and knowledge. It's more than a certificate, it symbolizes your dedication to professional growth.
EVERYTHING IN ONE PRICE
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AIDIFY COURSE SAMPLER: A PREVIEW OF OUR EXTENSIVE COURSE CATALOG
Explore examples of courses from the AIDIFY course catalog
- just a taste of what we offer
No courses matching current filter

Regulatory Affairs
Post-authorisation stage of the product lifecycle
Duration: 78 min course video

Regulatory Affairs
Introduction to referral procedures
Duration: 100 min course video

Regulatory Affairs
Naming of medicinal products
Duration: 89 min course video

Regulatory Affairs
Requirements for Product Information of medicinal products
Duration: 104 min course video

Regulatory Affairs
Managing Product Information updates depending on the type of procedure
Duration: 58 min course video

Regulatory Affairs
Introduction to excipients in labelling
Duration: 76 min course video

Regulatory Affairs
Mock-ups preparations
Duration: 83 min course video

Regulatory Affairs
Introduction to falsified medicines
Duration: 60 min course video

Regulatory Affairs
PIL readability testing
Duration: 73 min course video

Regulatory Affairs
Medicines under additional monitoring, the black triangle
Duration: 58 min course video

Regulatory Affairs
Procedures for authorizing medicines in the EU
Duration: 85 min course video

Regulatory Affairs
Dossier of authorized medicinal products in format of CTD, NeeS and eCTD
Duration: 83 min course video

Regulatory Affairs
Introduction to module 1 of registration dossier
Duration: 59 min course video

Regulatory Affairs
Regulatory Affairs in Poland
Duration: 87 min course video

Clinical Trials
Navigating EU CTR 536/2014 with transitioning from CTD
Duration: 113 min course video

Pharmacovigilance
Introduction to Medical Literature Monitoring
Duration: 88 min course video

Pharmacovigilance
Practical aspects of the review of the medical literature
Duration: 127 min course video

Pharmacovigilance
Medical Literature Monitoring based on journals review
Duration: 85 min course video

Pharmacovigilance
Global Medical Literature Monitoring
Duration: 159 min course video

Pharmacovigilance
Legal Regulations and Guidelines concerning Pharmacovigilance
Duration: 42 min course video

Pharmacovigilance
Introduction to Vaccine Safety Surveillance in EU
Duration: 83 min course video

Regulatory Affairs
Introduction to the activities performed by Regulatory Affairs Department
Duration: 47 min course video

Regulatory Affairs
Introduction to types of the procedures for registration of medicinal products
Duration: 49 min course video

Regulatory Affairs
Introduction to Module 2 of registration dossier
Duration: 33 min course video

Regulatory Affairs
Introduction to Module 4 of registration dossier
Duration: 17 min course video

Regulatory Affairs
Introduction to Module 5 of the registration dossier (Clinical study reports)
Duration: 28 min course video

Regulatory Affairs
Introduction to bioequivalence of medicinal products
Duration: 76 min course video

Regulatory Affairs
Introduction to data exclusivity and market exclusivity
Duration: 31 min course video

Pharmacovigilance
Introduction to Personal Data Protection in the pharmaceutical industry
Duration: 163 min course video

Pharmacovigilance
Practical aspects of Personal Data Protection in Pharmacovigilance and Clinical Trials
Duration: 264 min course video

Regulatory Affairs
Cosmetics registration
Duration: 104 min course video

Regulatory Affairs
Cosmetic product labelling
Duration: 66 min course video

Regulatory Affairs
Cosmetic Product Information File
Duration: 120 min course video

Pharmacovigilance
Cosmetovigilance
Duration: 48 min course video

Pharmacovigilance
Cosmetic product safety report and the role of the responsible person
Duration: 80 min course video

Pharmacovigilance
Management of Periodic Safety Update Report
Duration: 88 min course video

Pharmacovigilance
Introduction to role of Qualified Person Responsible for Pharmacovigilance
Duration: 88 min course video

Pharmacovigilance
Introduction to Pharmacovigilance Agreements and Service Provider Agreements
Duration: 113 min course video

Clinical Trials
Clinical trial documentation
Duration: 261 min course video

Clinical Trials
Introduction to planning and performing monitoring visits
Duration: 121 min course video

Clinical Trials
Documentation of monitoring visits
Duration: 159 min course video

Clinical Trials
Introduction to Site Selection Visit
Duration: 105 min course video

Clinical Trials
Site Selection Visit in practice
Duration: 123 min course video

Clinical Trials
Introduction to Site Initiation Visits
Duration: 142 min course video

Clinical Trials
Site Initiation Visit in practice
Duration: 126 min course video

Clinical Trials
Introduction to Site Monitoring Visits
Duration: 148 min course video

Clinical Trials
Site Monitoring Visit in practice
Duration: 102 min course video

Clinical Trials
eTools in clinical trials
Duration: 149 min course video

Clinical Trials
Introduction to informed consent
Duration: 315 min course video

Clinical Trials
Work with the informed consent
Duration: 260 min course video

Clinical Trials
Work with the clinical study protocol
Duration: 222 min course video

Clinical Trials
Introduction to Closeout Visits
Duration: 176 min course video

Clinical Trials
Introduction to Remote Monitoring Visits
Duration: 143 min course video

Clinical Trials
Management of an Investigational Product at a clinical site
Duration: 190 min course video

Clinical Trials
GCP: the most important updates with ICH GCP E6(R3)
Duration: 69 min course video

Clinical Trials
Introduction to Trial Master File
Duration: 67 min course video

Clinical Trials
Guidelines, regulations, and tools related to Trial Master File
Duration: 57 min course video

Clinical Trials
Introduction to Good Clinical Practice
Duration: 87 min course video

Clinical Trials
Good Clinical Practice — Advanced Course
Duration: 111 min course video

Clinical Trials
Good Clinical Practice from the Investigator's perspective
Duration: 149 min course video

Pharmacovigilance
Introduction to safety monitoring in clinical trials
Duration: 160 min course video

Pharmacovigilance
SUSAR, DSUR, PLL reports
Duration: 98 min course video

Pharmacovigilance
Introduction to organized post-marketing data collection systems
Duration: 109 min course video

Regulatory Affairs
CTD module 3 – Quality (EU). Active Pharmaceutical Ingredient (API) / Drug Substance in medicinal products for Human use
Duration: 231 min course video

Regulatory Affairs
CTD module 3 – Quality (EU). Medicinal products for Human use
Duration: 138 min course video

Clinical Trials
Preparation to audits and inspections in clinical trials
Duration: 113 min course video

Clinical Trials
Introduction to audit and inspection report
Duration: 47 min course video

Clinical Trials
Analysis of the audit and inspection report
Duration: 49 min course video

Clinical Trials
Introduction to CAPA Plan
Duration: 101 min course video

Clinical Trials
CAPA Plan Preparation
Duration: 106 min course video

Clinical Trials
Introduction to Quality Management System
Duration: 81 min course video

Clinical Trials
Quality Management System - how to create a good QMS
Duration: 106 min course video

Pharmacovigilance
The specifics of the Polish market in terms of the Risk Management Plan
Duration: 49 min course video

Pharmacovigilance
PRAC, CHMP, CMDh - the role and responsibilities that impact on the PV activities performed by MAH
Duration: 38 min course video

Pharmacovigilance
PSUR single assessment procedure and informal Work-Sharing procedure for follow-up for PSUSA for NAPs
Duration: 46 min course video

Pharmacovigilance
Introduction to the management of ICSRs
Duration: 154 min course video

Pharmacovigilance
Entering data into the Pharmacovigilance database system
Duration: 215 min course video

Pharmacovigilance
What is MedDRA and how is it used?
Duration: 76 min course video

Pharmacovigilance
Assessment and Medical Evaluation of ICSR
Duration: 106 min course video

Pharmacovigilance
How to prepare case narrative and sender's comment
Duration: 105 min course video

Pharmacovigilance
Management of Company Core Safety Information
Duration: 79 min course video

Pharmacovigilance
Management of Pharmacovigilance System Master File
Duration: 84 min course video

Clinical Trials
Introduction to competency model and career paths
Duration: 68 min course video

Clinical Trials
Introduction to individual development plan
Duration: 43 min course video

Pharmacovigilance
ChatGPT in the pharmaceutical industry
Duration: 247 min course video
