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.
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
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.
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).
- Board Certified Medical Affairs Specialist (BCMAS) (Certificate)
https://www.medicalaffairsspecialist.org/board-certified-medical-affairs-specialist-program
- Badge Board Certified Medical Affairs Specialist (BCMAS) (Badge)
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
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