Dassault Systèmes
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Contact
10 Rue Marcel Dassault
78140 Vélizy-Villacoublay
France
France Sales Representative
About us
We are Dassault Systèmes, a software company renowned for our commitment to balancing our actions and environmental impact. With 17,000 strategic partners, we hold the largest market share in the fields of PLM, 3D experience and clinical trial management, serving over 300,000 companies across 12 different industries.
Our deep conviction is that expanding and improving the real world through virtual means is essential for building a more sustainable future. Since 1981, our software solutions have played a crucial role in major scientific, industrial, ecological and societal transformations.
Our tools enable businesses to innovate responsibly, rethink their processes and make positive contributions to society while ensuring their competitiveness in the global market.
Business offer
Dassault Systèmes has an in-depth understanding of the challenges confronting pharmaceutical and biotech companies and is dedicated to assist these organizations with its vision to connect people and data in an organization and accelerating transformation through digital solutions across various domains:
- - Research & Discovery: Leveraging AI-based solutions to facilitate the discovery of new drugs and medicines, enhancing the efficiency and effectiveness of the research process.
- - Development: Streamlining laboratory operations by implementing standardized applications that seamlessly integrate lab equipment, materials, and procedures, thereby optimizing efficiency and productivity.
- - Tech Transfer: Maximizing data reuse and simulating production scenarios to ensure an efficient transition from development to manufacturing, focusing on factors such as quality, sustainability, yield, and cost-effectiveness.
- - Quality Management: Offering unique capabilities to create structured content and manage quality workflows throughout the entire lifecycle of a drug product, ensuring compliance and adherence to regulatory standards.
- - Clinical Trial Management: Providing innovative solutions such as synthetic control arms and tools for gathering patient feedback, facilitating the efficient and ethical management of clinical trials.
- - Manufacturing: Organizing data and creating a Virtual Twin of Biomanufacturing to optimize production processes, allowing for streamlined planning and execution while maximizing efficiency and resource utilization.
Activities
- Technology Supplier
- Other
- Target selection & validation
- Gene / protein discovery
- bioinformatics design
- Expression and pathway analysis of target
- quantification of target
- Assay development in in-vitro & in-vivo models
- Research exploratory companion biomarkers
- Hit discovery
- Screening & Identification
- Therapeutic libraries
- In silico
- In-vivo models
- In-vitro & ex-vivo models
- CMC
- GLP compliance
- GLP compliance
- Formulation
- Formulation
- Dose
- Stability
- Excipients
- Adjuvants
- Sterilization
- Lyophilization
- Storage stability
- Delivery
- Route of Administration
- Devices associated
- Regulatory filing
- Regulatory Filing
- Post-market surveillance
- Post-Market Surveillance
- Bioproduction engineering
- Cell Expansion
- Cell factory
- Process optimization
- Automated manufacturing
- On-line monitoring
- CGMP
- Bioproduction modeling
- Metabolic / Kinetic modeling
- Control / command
- Global optimization
- Economic analyses
- Artificial Intelligence tools
- Formulation
- Delivery
- Transport
- Supply chain logistics
- Tracking process
- Monitoring logistics
- Bioproduction/CMC/Analytical Quality Assessment, Quality Control
- Bioproduction
- Scale-Up
- Automated manufacturing
- Automated high throughput microbioreactor system
- Supply chain logistics
- Tracking process
- Monitoring logistics
- Non-GMP pilot batch
- GMP batch
- Cleaning
- CGMP
- Deviations
- Quality control
- CMC
- GLP compliance
- for preclinical NCS (non-clinical safety) studies
- viral safety testing
- GMP compliance
- Master Banks (cell and viral as needed)
- manufacturing
- Characterization and testing
- storage
- shipment
- Cell Culture / Fermentation
- media formulation and supply
- Bioreactor conditions (cell in suspension, adherent cell player)
- Ability to work in BSL2 conditions
- Bioproduction GMP
- Pilot Batches scale
- Process development & optimization
- Scale-Up & Validation
- Comparability characterization protocol
- Quality control & analytical process monitoring
- Stability Assessment
- Regulatory Filing
- Regulatory Filing
- New Drug Application (IND)
- Investigational Medicinal Product (IMPT) for clinical investigations (EMA)
- Common Technical document (CTD) section 3 (CMC) 4 (NCS) and 5 (Clinics) for submission
