Life Science Academy
LS Academy is a leading provider of specialized training, scientific events, and consulting services in the Life Sciences sector, including pharmaceuticals, medical devices, and clinical research. Since 2010, it has been committed to enhancing skills and knowledge through tailored courses, conferences, and expert support, with a focus on quality, innovation, and professional growth. The company collaborates with industry leaders, academic institutions, and medical associations to deliver high-impact educational programs and events, fostering continuous development and excellence in the industry.
Industries
Nr. of Employees
small (1-50)
Life Science Academy
Products
GMP / Pharmaceutical manufacturing training
Comprehensive courses covering GMP principles and manufacturing topics such as contamination control, Annex 1 compliance, aseptic process simulation, cleaning validation, supplier qualification and technology transfer.
Medical writing courses
Course portfolio for medical and regulatory writing including clinical study reports, protocols, DSUR/PSUR and communication for lay audiences.
Pharmacovigilance training portfolio
Courses addressing PV system implementation, case processing, signal detection and PSMF/inspection readiness.
Computer System Validation (CSV) training
Courses focused on CSV principles, GxP IT validation, audit and inspection considerations for regulated computer systems.
GxP cloud selection and validation course
Practical guidance on selecting, qualifying and validating cloud solutions to meet GxP requirements.
Aseptic Process Simulation (APS) course
Introduction and practical training on APS methodologies to support sterile manufacturing qualification and contamination control.
GMP / Pharmaceutical manufacturing training
Comprehensive courses covering GMP principles and manufacturing topics such as contamination control, Annex 1 compliance, aseptic process simulation, cleaning validation, supplier qualification and technology transfer.
Medical writing courses
Course portfolio for medical and regulatory writing including clinical study reports, protocols, DSUR/PSUR and communication for lay audiences.
Pharmacovigilance training portfolio
Courses addressing PV system implementation, case processing, signal detection and PSMF/inspection readiness.
Computer System Validation (CSV) training
Courses focused on CSV principles, GxP IT validation, audit and inspection considerations for regulated computer systems.
GxP cloud selection and validation course
Practical guidance on selecting, qualifying and validating cloud solutions to meet GxP requirements.
Aseptic Process Simulation (APS) course
Introduction and practical training on APS methodologies to support sterile manufacturing qualification and contamination control.
Services
Public and online courses across GMP, pharmacovigilance, medical writing, clinical research, regulatory affairs, medical affairs and statistics.
Customised training programs designed and delivered on-site or remotely for organisation-specific needs.
Operational support for preparation and organisation of investigator meetings including logistics and agenda coordination.
Preparation and editing of regulatory submissions, clinical study reports, safety documents and scientific communications.
Advisory services on regulatory strategy, market access, clinical development and operational readiness.
Full-service organisation of industry conferences, virtual events and networking activities tailored to life sciences topics.
Public and online courses across GMP, pharmacovigilance, medical writing, clinical research, regulatory affairs, medical affairs and statistics.
Customised training programs designed and delivered on-site or remotely for organisation-specific needs.
Operational support for preparation and organisation of investigator meetings including logistics and agenda coordination.
Preparation and editing of regulatory submissions, clinical study reports, safety documents and scientific communications.
Advisory services on regulatory strategy, market access, clinical development and operational readiness.
Full-service organisation of industry conferences, virtual events and networking activities tailored to life sciences topics.
Expertise Areas
- Training and professional development in life sciences
- GMP compliance and pharmaceutical manufacturing
- Quality risk management (ICH Q9) and deviation handling
- Pharmacovigilance and drug/device safety systems
Key Technologies
- Good Manufacturing Practices (GMP/cGMP) frameworks
- GxP documentation and quality systems
- Clinical trial regulations (ICH GCP, EU CTR)
- Pharmacovigilance systems and signal detection methods
News & Updates
A conference focused on pharmacovigilance in Germany.
A conference focused on pharmacovigilance in Germany.