Courses

Research into the basic science of cancer immunology has enabled us to harness the power of the immune system to treat cancer.
We are now entering a golden age of immunotherapy where new, sophisticated and innovative treatments are providing unprecedented cures for patients with advanced cancers. Chimeric antigen receptor (CAR) T cells are genetically engineered immune cells that can seek out and destroy cancer cells. So far, results have been very promising, but the use of CAR-T cells is associated with frequent, serious short-term toxicities. 

The 13th of March 2020, I have completed the course on Chimeric antigen receptor (CAR) T cells and earned the enclosed certificate.
I have conducted the course from the -Leukaemia Care organisation-, because I am interested
in finding new treatment alternatives and believe CAR-T cell treatment will be or is already
the "next generation" treatment. 

 (Certificate)

 

The course gives an overview of the field of CAR-T cells development, treatment and includes four (4) chapters.

  • Chapter 1: Introduction to CAR-T   

  • Chapter 2: Clinical Application of CAR-T cells  

  • Chapter 3: Practical Aspects of CAR-T

  • Chapter 4: Future Directions of CAR-T

 

https://leukaemiaelearning.org.uk/courses/car-t

Drug Safety, Pharmacovigilance, Pharmacokinetics, and Pharmacodynamics Training and Professional Certification Programs

 

Containing 3 different Programs and Batches 

Good Pharmacoepidemiology Practice Professional Certification Program (AV01B) (Certificate)

https://www.biopharmainstitute.com/LMS2018/badges/AV01B_Pharmacoepidemiology 

Drug Safety and Pharmacovigilance Professional Certification Program (AV01) (Certificate)

https://www.biopharmainstitute.com/LMS2018/badges/AV01_Safety and Pharmacovigilance


Pharmacokinetics and Pharmacodynamics Professional Certification Program (AV01A) (Certificate)

https://www.biopharmainstitute.com/LMS2018/badges/AV01A_PKandPD

Includes the Following Individual Courses

 

Drug Safety and Pharmacovigilance Professional Certification Program

Introduction to Drug Safety and Pharmacovigilance

Drug Safety: Signal Detection and Management in Pharmacovigilance

Drug Safety: Risk Management Planning for Medicinal Products

Drug Safety: Urgent Safety Restrictions

Drug Safety: Good Pharmacoepidemiology Practice

 

Pharmacokinetics and Pharmacodynamics Professional Certification Program

An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration

Conducting Pharmacokinetic and Pharmacodynamic Studies

I have conducted the course from the MIT Sloan School of Management and the MIT Computer Science and Artificial Intelligence Laboratory (CSAIL), completed this course and earned the enclosed certificate. 

(Certificate)

 

This 6-week (6 modules) program afford the opportunity to pioneer AI integration through an exploration of the core dimensions of key AI technologies, from a business and leadership perspective.

The course culminates in the development of a road-map for the strategic implementation of AI technologies in business.

 

Curriculum overview (details)

 

Module 1: An Introduction to Artificial Intelligence (AI)

Module 2: Machine Learning in Business

Module 3: Natural Language Processing (NLP) in Business

Module 4: Robotics in Business

Module 5: Artificial Intelligence (AI) in Business and Society

Module 6: The future of Artificial Intelligence (AI) 

 

The 8th of May 2019, I have completed the course on Essential Precision Medicine.

The Essential Precision Medicine course gives an overview of the field of precision medicine and includes the following modules:

 

  • Module PM 101: Human Genomics 

  • Module PM 102: Genes, Heredity and Disease 

  • Module PM 103: Genomics in Medical Practice 

 

https://precision-medicine-academy.thinkific.com/bundles/core-precision-medicine-series

The International Pharmaceutical Regulatory Affairs Professional Certification Program (PRA00A1)
(Certificate)

https://www.biopharmainstitute.com/LMS2018/badges/Regulatory Affairs

Includes the Following Individual Courses

 

Regulatory Affairs: Essentials for Human Medicinal Products (EU and US)

 Orphan Drug Designation in the USA and Europe

 Preparing Submissions in the Common Technical Document (CTD) format

Electronic Common Technical Document (eCTD)

Registration of Drugs Based on Monoclonal Antibodies

How to Gain Approval to Market Generic Drugs in the US

Submitting a New Drug Application (NDA) to Obtain Approval to Market in the US 

The European Centralized Procedure (CP) 

The Mutual Recognition Procedure (MRP) 

Variations to Marketing Authorizations in Europe 

The Decentralised Procedure (DCP) 

 

ICH GCP  E6  training 6 November 2019  (Certificate)

ICH GCP training 16 April 2019

ICH GCP training 11 October 2018

ICH GCP E6 Addendum (R2) training 15 June 2018

EU/GCP training 5 October 2017

 

 

 

The 19th April 2018, I have passed the Board Exam for the BCMAS (Board Certified Medical Affairs Specialist) Program and I am registered Board Certified Medical Affairs Specialist (BCMAS). 

https://www.medicalaffairsspecialist.org/board-certified-medical-affairs-specialist-program

 

 

The program includes the following 20 individual modules

 

Curriculum Overview (details)

The Pharmaceutical Industry

Medical Device Industry

Diagnostics Industry (IVD) (Certificate)

Rules Governing Interactions with Healthcare Professionals

Health Economics Outcomes Research (HEOR) (Certificate)

Evidence-Based Medicine (EBM)

Clinical Trial Designs

Presentation and Communication Skills

Regulatory Affairs

Compliance (Certificate)

Abstract and Medical Writing

Publication Practices

Drug Development Process

Medical Information

Medical Science Liaisons and Field Based Medical Teams

Grant and Investigator-Initiated Study Funding and Process

Advisory Boards 

Phase IV/Post-Marketing Studies

Risk Evaluation and Mitigation Strategies (REMS)

Medication Safety and Pharmacovigilance 

 

Introduction to the Biology of Cancer by Johns Hopkins University on Coursera

License number: UDJEMJ4MZR2L

https://www.coursera.org/account/accomplishments/certificate/UDJEMJ4MZR2L

Understanding Cancer Metastasis by Johns Hopkins University on Coursera

License number: JHYNQTJK39J6  

https://www.coursera.org/account/accomplishments/certificate/JHYNQTJK39J6

 

The Global Medical Device Regulatory Affairs Professional Certification Program Includes the Following Individual Courses

 

Medical Device Regulatory Affairs: Global

 Medical Device: Global Quality Management Systems (QMS)

 Medical Device: Global Risk Management