Medical Affairs
Date: December 17, 2024 (2 days) Price: 13 800 SEK per participant Place: Digitally Course Language: English Diploma: Certificate is awarded after completion of the course A course in Evidenced Based Marketing within the Pharma-, MedTech- and Biotech industry. Topics includes; Essentials in Health Economy, Swedish Health Authorities and their role(s), Compliance and Ethics, KOL-Development, Market Access and […]
Regulatory Affairs Advanced
Date: October 17 (1 day)Price: 6900 SEK per participantPlace: DigitallyCourse language: EnglishDiploma: Certificate is awarded after completion of the course This advanced course is a comprehensive extension of the RA essentials course and is relevant for those who need further insights in Pharmaceutical Development. This course will show how RA applies from early drug discovery and preclinical […]
Medical Affairs
Date: October 8, 2024 (2 days) Price: 13 800 SEK per participantPlace: Digitally Course Language: English Diploma: Certificate is awarded after completion of the course A course in Evidenced Based Marketing within the Pharma-, MedTech- and Biotech industry. Topics includes; Essentials in Health Economy, Swedish Health Authorities and their role(s), Compliance and Ethics, KOL-Development, Market Access and Lifecycle […]
Regulatory Affairs and Good Distribution Practice
Date: October 3, 2024 (1.5 days) Price: 10 350 SEK per participantPlace: Digitally Course Language: English Diploma: Certificate is awarded after completion of the course Comprehensive training on relevant regulations and guidelines to fully understand the requirements in submitting new MAs for Human Medicinal Products in Europe. In addition to this – how to optimize the life […]
Medical writing
Date: October 24 (1 day)Price: 6900 SEK per participantPlace: DigitallyCourse language: EnglishDiploma: Certificate is awarded after completion of the course This course will cover (1) Regulatory medical writing which will visualize and create the documentation that regulatory agencies require in the approval process for drugs, devices and biologics. This includes clinical study protocols, clinical study reports, patient […]
Good Manufacturing Practice
Date: October 1, 2024 (1 day) Price: 6900 SEK per participantPlace: Digitally Course language: English Diploma: Certificate is awarded after completion of the course The GMP training course provides an introduction and basic training with an overview of the pharmaceutical industry GMP standards. This course gives a solid understanding of how GMPs applies to the validation of […]
Good Clinical Practice
Date: October 22 (1 day)Price: 6900 SEK per participantPlace: DigitallyCourse language: EnglishDiploma: Certificate is awarded after completion of the course This comprehensive 6-hour course provides in-depth knowledge of Good Clinical Practice (GCP) principles, ensuring thorough understanding and adherence to the ethical and scientific quality standards for designing, conducting, recording, and reporting trials involving human subjects. The course […]
Good Manufacturing Practice
Date: December 10, 2024 (1 day) Price: 6900 SEK per participantPlace: Digitally Course language: English Diploma: Certificate is awarded after completion of the course The GMP training course provides an introduction and basic training with an overview of the pharmaceutical industry cGMP standards. This course gives a solid understanding of how GMPs applies to the validation of […]
Regulatory Affairs and Good Distribution Practice
Date: December 12, 2024 (1.5 days) Price: 10 350 SEK per participantPlace: Digitally Course Language: English Diploma: Certificate is awarded after completion of the course Comprehensive training on relevant regulations and guidelines to fully understand the requirements in submitting new MAs for Human Medicinal Products in Europe. In addition to this – how to optimize the life […]
Pharmacovigilance
Date: October 11 (1 day) Price: 6900 SEK per participantPlace: Digitally Course language: English Diploma: Certificate is awarded after completion of the course This course will provide an introduction to the essential principles and practices of pharmacovigilance, the science and activities related to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. […]