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5th Drug-Device Combinations & Sustainability Conference

  • 27th – 28th September 2023
  • Germany flag Germany Düsseldorf

The past decade has proved that the demand for sustainable medicine and compounds is no longer a manufacturing privilege, but a strong requirement for patient health and care for the environment.

This September we will bring together a dense variety of topics that will shed light on the current situation in the regulatory environment for drug-device combinations and sustainability of products.

The conference will gather experts from drug delivery fields, tunning on paperless submission, requirements, legislation, and introduction of new products. We will reach all the aspects that are needed to stay up-to-date, informed, and prepared for new challenges in the coming year.

Expand your knowledge and network on March 22-23, 2023, in Düsseldorf, Germany, at the 5th Drug-Device Combinations & Sustainability Conference, a great opportunity for communication with the pharmaceutical community.

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About the 5th Drug-Device Combinations & Sustainability Conference

The past decade has proved that the demand for sustainable medicine and compounds is no longer a manufacturing privilege, but a strong requirement for patient health and care for the environment.

In September we will bring together a dense variety of topics that will shed light on the current situation in the regulatory environment for drug-device combinations and sustainability of products.

The conference will gather experts from drug delivery fields, tunning on paperless submission, requirements, legislation, and introduction of new products. We will reach all the aspects that are needed to stay up-to-date, informed, and prepared for new challenges in the coming year.

Expand your knowledge and network on March 22-23, 2023, in Düsseldorf, Germany, at the 5th Drug-Device Combinations & Sustainability Conference, a great opportunity for communication with the pharmaceutical community.

Who Should Attend 

Executives, Directors, Heads, Leaders, Managers, Specialists, Engineers Professionals in Pharmaceuticals,

Principal Scientists, Principal Toxicologists, QC Laboratories, Manufacturers of Drug Substances (APIs), Contract Laboratories, Oral Solid Dosage Form, Clinical Research Org., Contract Research Org., Contract Manufacturing Org., Biopharma Companies, Biotechnology Prod., and Fellows specialising in: 

  • Chemistry 
  • External Supply 
  • Continuous Processing
  • Compliance
  • Manufacturing Science & Technology 
  • Regulatory Affairs 
  • Business Development 
  • Commercialisation
  • Quality Assurance/Control
  • Packaging
  • Licensing
  • Formulation Development 
  • Industrial Hygiene 
  • Health, Safety, & Environment (HSE)
  • Research & Development 
  • Compliance
  • Design Controls
  • Device Development & Manufacturing
  • Drug Delivery & Devices
  • Combination Products
  • Human Factors
  • Process Development
  • Strategic Development  
  • Risk Management 
  • Pharmaceuticals 
  • Biotechnology 
  • Plant Management
  • Usability Engineering
  • Device Engineering & Design
  • Operations 
  • New Products
  • Product Quality 
  • Drug Safety Evaluation   
  • Process Monitoring & Control 
  • Analytical Development Laboratories 
  • Internal & External Audit 
  • Training Departments 
  • Engineering 
  • Sterilisation
  • Vaccines
  • Validation 
  • Production
  • EHS  
  • QA/QC 
  • CMC 
  • CMO/CDMO 
  • Technology Transfer 
  • Other 

REQUEST A BROCHURE

To request an agenda for this Summit, please complete the details below. We will send you the agenda via email.

Key Practical Learning Points

  • Development of Drug-Device Combination Products
  • Premarket Review and Postmarket Regulations
  • Good Manufacturing Practice Regulations
  • Pharmaceutical Process Validation for Drug Devices
  • Regulatory Affairs and Quality Assurance   
  • Introduction of drug device combination product into DP development
  • Product Assignment of Combination Products
  • Achieving Cost Efficiency and Reducing Environmental Impact 
  • Technology-Based Approaches to Increasing Sustainability 
  • New Areas for Drug-Device Applications 

Francesco Malavasi, DE

Life cycle Engineering Specialist

Bayer

Francesco Malavasi, is Life cycle Engineering specialist at Bayer Ag., is responsible for reconstitution kits and other parenteral products, life cycle management.

With 14 years of experience in medical devices and Combination products, he gained experience in all the LCM stages, from development till commercialization, passing through post-launch phases and scale-up activities.

Throughout his career, he has been involved in the development and commercialization of Autoinjectors, kits, Pen injectors, and other parenteral devices.

Francesco, besides an aeronautical background, holds a Bachelor in Engineering Management.

Troels Keldmann, DK

Advisor and Interim Technical Lead

Keldmann Healthcare A/S

Dr. Troels Keldmann has spent 25 years in the DDS devices and medical devices industry, working cross-functionally covering development, sourcing, innovation, IPR strategy, business development, partnering, and commercialisation. As interim technical lead on injection devices at LEO Pharma A/S, he headed identification, evaluation, and selection of SC injection devices. His prior DDS experience includes co-founding and heading innovative DDS startups, and consulting in DDS devices for pulmonary, nasal, SC (needle/needle-free), and IM delivery. He is an appointed business coach by the European Innovation Council and an industry fellow at Technical University of Denmark. He holds a BSc, MSc and PhD in mechanical engineering and innovation, as well as an MBA.

Francesco Malavasi, DE

Life cycle Engineering Specialist

Bayer

Troels Keldmann, DK

Advisor and Interim Technical Lead

Keldmann Healthcare A/S

BROCHURE

Request the 5th Drug-Device Combinations & Sustainability Conference brochure and find out the latest topics and ideas that will be shared.  

Request

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