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JOIN US IN OUR MISSION TO REVOLUTIONIZE EMPLOYEE DEVELOPMENT IN THE PHARMA INDUSTRY

We empower your career, offering unlimited learning, competence-based education, and practical real-world training

Unlimited Learning, One Price

Gain full access to comprehensive content across CT, RA, and PV. With about 120 hours of engaging video and other extensive resources, our subscription offers exceptional value and a wealth of knowledge at your fingertips.

Credible Learning with References

Each AIDIFY course integrates references ensuring the accuracy and reliability of the content. This enables you to verify the accuracy of the information, access additional resources, broaden understanding, and enhance critical thinking skills.

Learning That Fits Your Life

Embrace the convenience of AIDIFY's video microlearning. Our bite-sized lessons are designed to fit seamlessly into your busy schedule, making it effortless to continue learning and growing, no matter where you are.

Competence-Based Learning

Our courses are structured to match your career path, focusing on the skills and knowledge needed for specific job roles. Each part of the course targets real-world problems, making sure what you learn directly helps your career progress.

Practical, Real-World Training

Our courses are not just about theory; they're about practical application. Each course include hands-on activities crafted to develop skills that you can directly apply in real-world scenarios. This approach ensures you're equipped for success.

Confirm Your Expertise

Upon completing AIDIFY courses and passing tests, earn certificates that validate your qualifications, understanding of relevant GxP requirements, as well as adequate experience for the assigned tasks and responsibilities.

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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Competences
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

Regulatory Affairs

Post-authorisation stage of the product lifecycle

Duration: 78 min course video

Regulatory Affairs

Variation as a tool to implement a change

Duration: 114 min course video

Regulatory Affairs

Introduction to referral procedures

Duration: 100 min course video

Regulatory Affairs

Rules of variation grouping

Duration: 52 min course video

Regulatory Affairs

Fees payable to Regulatory Agencies on the example of EMA and URPL in Poland

Duration: 60 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: 62 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

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

Wprowadzenie do ochrony danych osobowych w branży farmaceutycznej

Duration: 163 min course video

Pharmacovigilance

Praktyczne aspekty ochrony danych osobowych w pharmacovigilance i badaniach klinicznych

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

Additional risk minimization measures

Duration: 97 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 Risk Management Plan

Duration: 95 min course video

Pharmacovigilance

Management of Risk Management Plan

Duration: 151 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

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

Polish Health Authority requirements for additional risk minimization measures

Duration: 38 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

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

Regulatory Affairs

Introduction to competency model and career paths

Duration: 68 min course video

Clinical Trials

Introduction to individual development plan

Duration: 43 min course video

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